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SEOUL, South Korea, Oct. 3, 2024 /PRNewswire/ -- Panacell Biotech Co., Ltd. (Panacell Biotech) announced that the patent related to their exosome manufacturing method filed last year was registered as a core technology in the patent registry on August 7, 2024, following the Patent Act. Panacell Biotech, whose Chief Executive Officer (CEO) is Dr. Seung Ho Choi, is a research institute specializing in stem cells and a cell processing institution certified by the Ministry of Food and Drug Safety. Panacell Biotech research results Panacell Biotech has filed three patents on cosmetic compositions containing exosomes produced using established methods for manufacturing exosomes derived from natural killer (NK) cell culture supernatant, adipose-derived stem cell (ADSC) culture supernatant, and whey protein-derived exosomes (WP-EXO). Among these, the company registered the patents for the manufacturing method of exosomes derived from NK cell culture supernatant and the cosmetic composition containing exosomes produced using this method. In addition, a patent application is underway for the recently established core technology of manufacturing exosomes derived from Wharton's jelly mesenchymal stem cells (WJ-MSCs). The core of Panacell Biotech's exosome manufacturing patent is the separation of exosome particles up to 4×10¹¹ (400 billion)/mL using a filtration method from the culture medium obtained during the co-culture process of NK cells, NKT cells, and T cells extracted from a patient's adipose tissue or blood. The filtration device employs a method suitable for high-concentration samples by forming a fluid flow parallel to the filtration membrane to prevent fouling on the membrane surface. This method has been proven by extracting ultra-high-concentrated exosomes and analyzing them through the western blot. Dr. Seung Ho Choi stated that, beyond treating domestic patients, the company has secured stem cell-related technology to a completion stage. With this technology, they recently attracted an investment of $5 million from the United States. They also signed memorandums of understanding to promote international technology transfers worth $12 million each to Malaysia and China. Panacell Biotech also discovered multiple exosomes within the culture medium through component analysis. They have secured technologies for filtration, storage, mass production, and inspection for export and are currently operating a subsidiary established in New York. Dr. Seung Ho Choi said, "Based on our experience researching and developing exosomes derived from human cells, we expect to see the fruition of developing therapeutics for rare and intractable diseases. We can achieve this by jointly working with domestic and international research institutions and medical organizations to create exosomes loaded with small interfering ribonucleic acid (si-RNA) that inhibits messenger RNA (mRNA) protein synthesis, utilizing exosomes as the core technology." Exosome cosmetics contain exosomes, nano-sized particles secreted by cells that include various bioactive substances such as proteins, nucleic acids, and lipids. These bioactive substances can exhibit multiple skin improvement effects, including skin regeneration, anti-inflammation, anti-oxidation, and whitening. Since the effects of exosomes replicate the characteristics and functions of the original cells and vary significantly with concentration, the functionality of the cosmetics can also differ. Exosomes have a high skin absorption rate and can deliver bioactive substances to the deeper layers of the skin. With a structure similar to cells, they possess high skin compatibility and can solve the problem of low absorption rates of 1–3% caused by skin structure.
Organizations Plan to Jointly Advance Breakthrough Solutions in Human Health and Sustainability, Drive Research Collaboration, Entrepreneurship and Accelerate Talent Development SINGAPORE, Oct. 3, 2024 /PRNewswire/ -- The Agency for Science, Technology and Research (A*STAR), Singapore's lead public sector R&D agency, and Flagship Pioneering, the bioplatform innovation company, today announced plans to collaborate to advance health and sustainability outcomes in Singapore and the broader Asia Pacific region. In this collaboration, A*STAR and Flagship will jointly commit up to SGD100 million over the next five years. A*STAR and Flagship outlined the goals of their collaboration via a Memorandum of Understanding (MOU) signed Tuesday. The collaboration will promote research and development activities between A*STAR research institutes and Flagship portfolio companies, to co-develop technologies in strategically important areas. Talent development is another pillar of the collaboration, with potential scientific dialogues and internship opportunities at Flagship and its portfolio companies. Together, A*STAR and Flagship seek to spur innovation and venture creation activities that help create and grow Flagship companies in Singapore. Flagship will contribute its signature approach to company creation and development while A*STAR will contribute its expertise in science and technology through access to its scientists and facilities. This MOU will have the potential to expand and foster collaborations among key players across Singapore's biotech ecosystem. "By joining forces, Flagship and A*STAR can further boost the already thriving life sciences ecosystem in Singapore and beyond, with breakthrough research, purposeful entrepreneurship and accelerated talent development," said André Andonian, Chair of Asia Pacific and Strategic Advisor, Flagship Pioneering. "This collaboration blends scientific acumen and entrepreneurial spirit and will further accelerate and expand Flagship's impact globally. We are pleased to announce this collaboration with A*STAR within the first year of opening our new Asia Pacific hub, located in Singapore." "We are excited to be working with globally-recognized venture builders like Flagship Pioneering, to bring new companies with cutting-edge technologies in areas of strategic interest to Singapore," said Irene Cheong, Assistant Chief Executive at A*STAR's Innovation & Enterprise Group. "This collaboration is a key step in nurturing our entrepreneurial talent and exploring new, innovative approaches to venture building. As we continue to expand these partnerships, we are confident that they will drive significant growth in Singapore's innovation landscape and advance Singapore's position as a global hub for biotechnological innovations." About the Agency for Science, Technology and Research (A*STAR) The Agency for Science, Technology and Research (A*STAR) is Singapore's lead public sector R&D agency. Through open innovation, we collaborate with our partners in both the public and private sectors to benefit the economy and society. As a Science and Technology Organisation, A*STAR bridges the gap between academia and industry. Our research creates economic growth and jobs for Singapore, and enhances lives by improving societal outcomes in healthcare, urban living, and sustainability. A*STAR plays a key role in nurturing scientific talent and leaders for the wider research community and industry. A*STAR's R&D activities span biomedical sciences to physical sciences and engineering, with research entities primarily located in Biopolis and Fusionopolis. For ongoing news, visit www.a-star.edu.sg. About Flagship Pioneering Flagship Pioneering invents and builds bioplatform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in more than $75 billion in aggregate value. To date, Flagship has deployed over $3.8 billion in capital toward the founding and growth of its pioneering companies alongside more than $27 billion of follow-on investments from other institutions. The current Flagship ecosystem comprises 40 companies, including Foghorn Therapeutics (NASDAQ: FHTX), Moderna (NASDAQ: MRNA), Omega Therapeutics (NASDAQ: OMGA), Sana Biotechnology (NASDAQ: SANA), Generate Biomedicines, Inari, Indigo Agriculture, and Tessera Therapeutics. Media Contacts: Flagship Pioneeringpress@flagshippioneering.com A*STARNicolette_Ng@hq.a-star.edu.sg
SK bioscience completed the acquisition of German CDMO company IDT Biologika with over a century of history that enables immediate expansion in revenue and infrastructure. The company aims to double sales of IDT Biologika by 2028 through new business projects and operational efficiency. The company will invest in high-growth businesses such as stage cell and gene therapy (CGT) and recombinant vaccine. SK bioscience will accelerate its global push based on the complementary capabilities of both companies. SEONGNAM, South Korea, Oct. 2, 2024 /PRNewswire/ -- SK bioscience, a global innovative vaccine and biotech company committed to promoting human health from prevention to cure, today announced the successful completion of its acquisition of a controlling stake in a German company, IDT Biologika, one of the top 10 global vaccine contract development manufacturing organizations (CDMO). (from left) SK bioscience President and CEO Jaeyong Ahn and Klocke Group CEO Carsten Klocke on the signing ceremony in June In June 2024, SK bioscience has signed an agreement with Klocke Group, a German biopharmaceutical group, to acquire a controlling stake in IDT Biologika, Klocke Group's affiliate. As part of this transaction, Klocke Group will retain a 40% stake in IDT Biologika while investing approximately KRW 76 billion to acquire a 1.9% stake in SK bioscience. This cross-shareholding agreement is designed to strengthen their partnership, which is built on mutual trust in each company's operational capabilities and growth potential. With the acquisition complete, SK bioscience is set to focus on promoting the organic and systematic integration of both companies to enhance management efficiency and drive business expansion. The company plans to double IDT Biologika's annual sales by 2028 and improve its EBITDA (earnings before interest, taxes, depreciation, and amortization), targeting up to 25% of its sales. Leveraging the benefits of the IDT Biologika acquisition, SK bioscience also aims to achieve KRW 1 trillion (appx. USD 757.6 million) in consolidated sales within the next five years. The company's growth is expected to accelerate with the launch of next-generation pneumococcal vaccines, fueling its further expansion beyond 2028, and to see the significant improvements in its financial performance. The company will first seek to maximize the utilization rate of IDT Biologika's manufacturing facilities. In particular, the company plans to increasingly utilize some of IDT Biologika's DS (drug substance) and DP (drug product) high-performance production lines, such as the large-dose vial line, for potential major projects with global pharmaceutical companies. In addition, the company will optimize the lyophilized vial line to extend the existing contracts and win contracts for promising clinical pipelines and late-stage cell and gene therapy (CGT) projects. With additional cell line manufacturing and recombinant vaccine development technology, the company plans to pursue new CDMO contracts for mid- to large-scale products. SK bioscience will also invest in high-growth businesses such as the pre-filled syringes (PFS), recombinant vaccine, and CGT, which includes oncolytic viruses (OV), adeno-associated viruses (AAV), and lentiviruses (LV). Additionally, the company will transfer its technology and production to IDT Biologika for key products such as flu, shingles, chickenpox, and typhoid vaccines. Moving forward, SK bioscience undertakes key initiatives to improve IDT Biologika's short-term operational efficiency and profitability, including enhancing batch operational efficiency and raw material management, streamlining the supply chain, and improving quality management and operational management. SK bioscience believes that, given IDT Biologika's proven track record of technology and expertized talents, business expansion and operational improvements will proceed swiftly. IDT Biologika has maintained long-standing CDMO partnerships with over 15 of the world's major biotech and pharmaceutical companies, as well as research institutions. In addition to manufacturing vaccines for viral diseases such as COVID-19, the company has experience in contract manufacturing of various biopharmaceuticals. Takeda is one such company that IDT has partnered with many years for its dengue vaccine. Moreover, IDT Biologika has also the capability to expand into the CGT business especially as the producer of one of the few worldwide FDA and EMA-approved oncolytic viral therapies of a global player. The CGT business is one of the future growth engines of SK bioscience. To ensure rapid management stabilization and synergies, key executives from both companies including Carsten Klocke, CEO of the Klocke Group, and Jaeyong Ahn, President and CEO of SK bioscience, will serve on IDT Biologika's Advisory Board. The advisory board will ensure IDT Biologika's independent management while carrying out cultural integration. Dr. Sally Choe, Head of Development HQ of SK bioscience, has been named as co-CEO of IDT Biologika along with Dr. Ulrich Valley. Dr. Choe, who holds a Master and Ph.D. in Pharmaceutics from the University of Michigan, has worked for global pharmaceutical companies such as Pfizer-Bristol-Myers Squibb (BMS) and Parexel Regulatory Consulting firm. She has 12 years of tenure at the U.S. Food and Drug Administration (FDA), where she served as a Deputy Director in the Office of Translational Sciences (OTS) and as Super Office Director of the Office of Generic Drugs (OGD). Dr. Ulrich Valley, Co-CEO of IDT Biologika, said, "I am convinced that this milestone will contribute to future growth and to our vision of a leading CDMO. This global strategic cooperation is an important driver for our innovative strength, competitiveness and sustainable success, built on a foundation of trust and common goals. I am certain that we, SK bioscience and IDT Biologika, can achieve great things together by combining our competences and capabilities." Jaeyong Ahn, President and CEO of SK bioscience, said, "With the successful completion of IDT Biologika acquisition, we are rapidly stabilizing management as SK bioscience and IDT Biologika now unite one family. The capabilities of the two companies are expected to generate significant synergies, and we will accelerate our global expansion." About SK bioscience SK bioscience is an innovative vaccine and biotech company, committed to vaccine development and manufacturing to enable more equitable access to vaccines around the world. Leveraging strengths on cutting-edge technologies, SK bioscience has been dedicated to promoting human health from prevention to cure across the globe. With the cooperation of domestic and international governments, regulatory agencies, healthcare providers, doctors, and medical experts, all of the SK colleagues are passionately committed to providing high-quality vaccines to those who need them and better public healthcare solutions. - SK bioscience Website- SK bioscience Linkedin ContactSK bioscience Communications TeamChanghyun Jin(jin99@sk.com)Jeannie S. Pak(j.pak@sk.com)
TOKYO, Oct. 1, 2024 /PRNewswire/ -- PeptiGrowth Inc. (Headquarters: Chiyoda-ku, Tokyo; President: Jiro Sugimoto) has successfully developed a novel synthetic peptide called "FGF2 alternative peptide (FGFR1c agonist)", which has equivalent function to recombinant FGF2 (Fibroblast Growth Factor 2, basic FGF (bFGF)). This product will be on the market at the beginning of October 2024. Development of Synthetic Peptide Growth Factors by PeptiGrowth Traditional growth factors and cytokines used in regenerative medicine and cell therapy manufacturing face several quality issues, including lot-to-lot variability, potential contamination with biological impurities, low stability, and high costs. PeptiGrowth has focused on developing a series of synthetic peptides that address these challenges while maintaining functionality equivalent to conventional growth factors and cytokines. Their peptides are completely chemically synthesized and free from animal components, enabling the formulation of xeno-free and chemically defined cell culture media. About FGF2 alternative peptide (FGFR1c agonist) [Product code: PG-011] The FGF2 Alternative Peptide (PG-011) is a dimeric peptide composed of cyclic peptides that bind to human FGFR1c. PG-011 exhibits agonist activity toward FGFR1c by binding to it, thereby activating signaling pathways in various cell types. Conceptual Diagram of the Mechanism of Action of PG-011 PeptiGrowth has confirmed that PG-011 promotes the proliferation of human mesenchymal stem cells (MSCs) at approximately one-third the concentration of FGF2 when compared on a ng/mL basis. Additionally, in collaboration with the CiRA Foundation, they evaluated PG-011's ability to maintain the undifferentiated state of human iPSCs. Three iPSC lines were cultured for 7 days in media containing either 100 ng/mL (~5.9 nM) of FGF2 or the same molar concentration (equivalent to ~30 ng/mL) of PG-011, followed by three passages. Afterward, cell morphology observations and undifferentiated marker measurements were conducted. Following three passages, iPSCs cultured in both PG-011 and FGF2 exhibited nearly identical morphology. Furthermore, analysis of undifferentiated markers (SSEA4 and TRA-1-60) indicated that iPSCs cultured with PG-011 displayed a similar positivity rate to those cultured with FGF2. Cell proliferation rates during the culture period were also equivalent under both conditions. These results suggest that PG-011 has the ability to maintain iPSCs in an undifferentiated state, comparable to FGF2. Proliferation of human MSCs by PG-011 and observations of cell morphology of iPSCs after 3 passages of culturing in the presence of PG-011 or FGFs, as well as the measurement of undifferentiated markers on Day 7 at P3. Recombinant FGF2 is known for its low stability, as it degrades and loses activity easily under culture conditions. This necessitates higher concentrations and frequent medium changes, significantly increasing production costs and workload. PeptiGrowth has confirmed that PG-011 maintained its full activity even after 4 days of incubation at 37°C, whereas FGF2's activity significantly declined under the same conditions, demonstrating the superior stability of PG-011. Moreover, they assessed the reactivity of PG-011 with bovine cells, as FGF2 is a key growth factor in cultivated meat production. PG-011 efficiently promoted the proliferation of bovine muscle satellite cells, suggesting that PG-011 may demonstrate cross-reactivity across various cell types, including those of non-human origin, making it a promising candidate for use in cultivated meat production. PG-011 provides cell proliferation and undifferentiated state maintenance comparable to FGF2 but with superior stability, reducing both usage costs and workload. It also shows excellent proliferation activity in both human and bovine cells, making it a compelling choice for regenerative medicine and cultivated meat production. Product Overview Product name: FGF2 alternative peptide (FGFR1c agonist)Product code: PG-011Product form: LyophilizedStorage conditions: -20°C or lessPurity: ≥95% by HPLCMolecular weight: 5127.81(Acetate)Size: 10 µg, 50 μg (volume per glass vial) *This product can be provided with an Animal Component Free (ACF) certificate.*This product is for testing and research use only (RUO).*There is a possibility that the specifications can change. Purchase Our Product If you would like to purchase our products, please contact us using the information below. For customers who would like to purchase GMP compliant products as well as the above PG products in bulk scale, please contact us using the information below. Development of other peptides from PeptiGrowth We have developed alternative peptides targeting numerous growth factors and cytokines. To date, we have launched 11 products and plan to launch several additional growth factor alternative peptides targeting PDGF-AA, KGF, and IL-15 between late 2024 and mid- 2025. Details will be updated on our website (https://peptigrowth.com/en/) . If you are interested, please contact us using the following contact information. Contacts for inquiries or additional information: PeptiGrowth Inc. E-mail: contact@peptigrowth.com TEL：+81-70-4503-1497
-- Founding CEO Mark Clein named Executive Chairman; Mr. Clein and co-founder Ethan Leder to continue as Board Directors -- BETHESDA, Md., Oct. 1, 2024 /PRNewswire/ -- Precision Medicine Group (Precision), a leading next-generation provider of drug development and commercialization services, today announced the appointment of Margaret Keegan as Chief Executive Officer (CEO) and member of the Board of Directors, effective immediately. Ms. Keegan succeeds Mark Clein, who is assuming the role of Executive Chairman. Mr. Clein co-founded Precision in 2012 as CEO and, together with co-founder Ethan Leder, purpose-built Precision to capitalize on the scientific and technological innovations that are transforming drug development and enabling widespread access to new, breakthrough therapies. Mr. Leder formerly served as Executive Chairman and will remain a member of the Board of Directors. Today, Precision is a global team of 3,500 experts spanning the clinical through commercial continuum, and operating across two groups: Precision for Medicine, the premier provider of biomarker-driven clinical research and development, including integrated lab and clinical trial services, and Precision AQ, the foremost provider of commercialization services supporting life science organizations from launch through product maturity. "We founded Precision with the belief that we could help change the healthcare landscape by improving the development and commercialization of new therapies and supporting access to life-changing medicine for every patient, everywhere. Over the past dozen years, we invested in the necessary capabilities to power this vision, and I am grateful to my colleagues who work tirelessly to meet the dynamic needs of biotechnology and pharmaceutical companies," said Mark Clein, Co-founder and Executive Chairman of Precision. "Together, we supported the development and launch of hundreds of therapies for some of the most intractable and devastating diseases and provided life science companies the insights, tools, and resources to navigate a complex and ever-evolving global healthcare industry. In Margaret Keegan, we have identified a leader with the vision, experience, and acumen to architect the next chapter. Ethan and I look forward to working with her to further deliver on our purpose for our clients, employees, and the patients they serve." Margaret Keegan, Chief Executive Officer, commented, "Precision was among the first to recognize the power of more personalized, targeted therapies to deliver better outcomes, and early to identify the possibilities and challenges that precision medicine-based approaches would introduce from clinical development through commercialization. In many ways, our industry is at a similar inflection point now, as we assimilate innovations in technology and artificial intelligence and respond to new regulations and shifting macroeconomic conditions. This introduces a tremendous opportunity for Precision to advance from being the first mover in precision medicine to being the global expert in drug development and commercialization. I am thrilled to be joining Precision at this exciting point in the company's rapid development and look forward to leading this outstanding team of professionals." "Our selection of Margaret as the next CEO of Precision is the result of a long-term succession planning process. Margaret is a passionate leader, with extensive and proven life sciences industry experience. She has a deep commitment to our foundational principles, with a focus on our patient-centric and client-first approach. The Board is confident in her ability to grow and scale Precision as a complete development partner for our biopharmaceutical customers, from clinical R&D through commercialization," said Dr. John Hubbard, Chairman of the Precision Board of Directors. "On behalf of the Board, I want to express my gratitude to Mark and Ethan for their leadership over the last 12 years. In addition to architecting our innovative business model, they've built an industry-leading team and culture that positions Precision for continued success. I know Mark and Ethan will be active contributors on the board as they transition into their new roles." About Margaret Keegan, CEO of Precision Medicine Group Ms. Keegan is an industry luminary, who has held executive leadership roles at large pharmaceutical and leading life sciences companies. Most recently, Ms. Keegan served as Operating Partner at Linden Capital Partners, where she evaluated opportunities across the sector, including providers of clinical research, pharmaceutical and commercial services. Prior to joining Linden Capital Partners, Ms. Keegan was the Executive Vice President, Chief Operating Officer at PRA Health Sciences, where she held sole responsibility for managing the business operations through the sale of the business to ICON plc. Earlier, Ms. Keegan spent over a decade at IQVIA, where she held roles of increasing responsibility, including President – Clinical Development, responsible for global clinical trials and President, Data Management, Biostatistics, Central Monitoring, Safety and Regulatory. Ms. Keegan launched her career in life sciences at GlaxoSmithKline. Ms. Keegan holds a B.Sc. with First Class Honours in Mathematics from the University of Strathclyde and was named a Chartered Statistician by the Institute of Statisticians, United Kingdom. About Precision Medicine GroupFormed in 2012, Precision Medicine Group is a specialized services company supporting next-generation approaches to drug development and commercialization. Precision provides an integrated infrastructure that supports pharmaceutical and life science companies as they develop new products in the age of precision medicine. The company is headquartered in Bethesda, Maryland, with offices throughout North America, Europe and Asia. For more information, visit precisionmedicinegrp.com. ContactHannah DeresiewiczPrecision AQhannah.deresiewicz@precisionaq.com Logo - https://mma.prnasia.com/media2/2504517/Precision_Medicine_Group_Logo.jpg?p=medium600
SYDNEY, Oct. 1, 2024 /PRNewswire/ -- Great Place To Work® ANZ, the global authority on workplace culture today announces their inaugural 15 Best Workplaces™ in Healthcare, Social Assistance and BioPharma in 2024. The companies are announced across two lists: Best Workplaces in Biotechnology and Pharmaceuticals (Biopharma) and Best Workplaces in Healthcare and Social Assistance (which covers two categories Medium & Large and Small & Micro). Category sizes include – micro (companies with less than 30 employees), small (companies with 30 to 99 employees), medium (companies with 100 to 999 employees), and large (companies with 1,000 or more employees). The companies were shortlisted using rigorous analytics and confidential employee feedback. In curating what makes a Best Workplace in Australia, we have used the same methodology as we do in curating the renowned Fortune 100 Best Companies to Work For in the US and Fortune's World's Best Workplaces. Rebecca Moulynox, General Manager of Great Place To Work Australia, emphasised the value of recognising excellence across specific industries on a national stage. "We understand that different industries face unique challenges and opportunities," Moulynox said. "To celebrate organisations that are making significant strides within their sectors, we've introduced new industry-specific lists in 2024, including Best Workplaces in Healthcare & Social Assistance and Best Workplaces in Biotechnology & Pharmaceuticals." "These lists provide a fantastic opportunity to spotlight companies that excel in creating a positive workplace culture within their industry. It's a chance to honour those who are dedicated to enhancing employee experiences, fostering inclusivity, and driving progress in their fields." "By highlighting organisations committed to ensuring their employees feel safe, valued, and heard, we aim to inspire others to elevate their workplace practices and continue advancing the standards of great workplaces across Australia," she added. About Great Place To Work® Great Place To Work® is the global authority on workplace culture. Our mission is to help every place become a great place to work for all. We give leaders and organisations the recognition and tools to create a consistently and overwhelmingly positive employee experience, fostering cultures that are proven to drive business, improve lives, and better society. Our recognition is the most coveted and respected worldwide for elevating employer brands to attract the right people. Our proprietary methodology and platform enable organisations to truly capture, analyse, and understand the experience of all employees. Our groundbreaking research empowers organisations to build cultures that retain talent and unlock the potential of every employee. Our coaches, content, and community connect the boldest leaders, ideas, and innovations in employee experience. Since 1992, our Certification™, Best Workplaces™ Lists, and global benchmarks have become the industry standard, built on data from more than 100 million employees in 150 countries around the world. About Great Place To Work Certification™ Great Place To Work® Certification™ is the most definitive "employer-of-choice" recognition that companies aspire to achieve. It is the only recognition based entirely on what employees report about their workplace experience—specifically, how consistently they experience a high-trust workplace. Great Place To Work Certification is recognised worldwide by employees and employers alike and is the global benchmark for identifying and recognising outstanding employee experience. Every year, more than 10,000 companies across 60 countries apply for Great Place To Work Certified. Embargoed till 9:00AM AEST, 1 October, 2024 Australia's Best Workplaces™ in Healthcare & Social Assistance in 2024 ListMicro & Small Category RANK COMPANY 1 Spine & Sports Physiotherapy 2 Adam Dental 3 Holistic Recovery 4 Unify Disability Services 5 Unbound Minds Australia's Best Workplaces™ in Healthcare & Social Assistance in 2024 ListMedium & Large Category RANK COMPANY 1 Medtronic Australasia Pty Ltd 2 Pinnacle Rehab 3 Avenue Dental 4 Just Better Care 5 Arjo Australia Australia's Best Workplaces™ in Biotechnology & Pharmaceutical in 2024 List RANK COMPANY 1 AbbVie Pty Ltd 2 Sandoz 3 Glaukos 4 Lundbeck Australia Pty Ltd 5 Servier Australia
Biotechnology
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