Asia Empowering Medical Professionals With The Latest Technology
Medical Devices are considered a fundamental component of Health Systems; the benefits they can provide continue to increase as they're essential to prevent, diagnose, treat and rehabilitate illnesses and diseases in a safe and effective way. The steps that involve Medical Devices manufacturing, regulation, planning, assessment, acquisition, and management are complex but essential to guarantee their quality, safety and compatibility with the settings in which they are used. Pharmaceutical regulation is designed to ensure safety, efficacy, and quality of the drugs available to consumers....
Our subscribers play a decisive role in finalization of our annual list of "Top 10 Most Promising Medical Device & Pharmaceutical Regulatory Consultants From Asia - 2023" by nominating those which have served them with excellence and are praiseworthy. If you feel there is a company that deserves to be on our annual list, do write to us about them mentioning their value proposition.
A health care & pharmaceutical consulting company assisting the clients acquire imports of pharmaceutical raw materials, pharmaceutical equipment, laboratory equipment, medical devices and other products
A regulatory representative specialising in product registration with the saudi food & drug authority (SFDA) and local markets access for international manufacturers of medical devices and pharmaceuticals
A regulatory solutions provider serving the drugs, medical devices, biological, IVDs, neutraceuticals, food, and cosmetic industries
A comprehensive regulatory consultancy company providing solutions to maintain their competitive advantage from early stage of product development to through out the life cycle of the product
A provider of 360° pharma regulatory and quality service company offering expert consulting services & cutting-edge software solutions to streamline all your pharma regulatory & quality processes
A highly focused GxP compliance and regulatory affairs service oriented company that supports the toughest GxP compliance and regulatory affairs challenges
A life sciences consulting company offering end to end product development consulting services including regulatory affairs, pharmacovigilance, clinical trials and medical writing services to the clients
A service provider which offers regulatory affairs services, impurities supply, technical writing and translation services to pharmaceutical companies and clinical research organizations (CRO)
An expert medical device company providing assistance for the company which need to be certified with good distribution practice for medical device (GDPMD), ISO 13485 : 2003 and also medical device registration assistance in malaysia
A service provider for complete solution on pharmaceutical product dossier registration, regulatory affairs support and its marketing, with rich experience in product selection, dossier compilation, registration of the product, post registration marketing on various models
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