NAMSA clinical regulatory consultants have substantial practical experience of compiling and examining complex documentation and medicinal material dossiers (the Frequent Specialized Doc [CTD structure]) for drug/device solutions. This experience ranges from wound dressings to heart valves and drug coated stents.
Whether you require assistance with document compilation for the regulatory submission or a gap Examination overview prior to submitting towards your Notified Overall body, NAMSA is here that can help!
Access the best cGMP expert The 1st time—anywhere and when you want them. Discovering major GxP talent from the hyper-aggressive lifetime science industries will get tougher on a daily basis.
Tap into numerous competencies and skillsets for any predetermined or open up-finished period of time based upon your evolving requirements.
Get entry to qualified consultants and contingent or direct hire candidate search and placement services. We concentrate on the entire range of the resourcing procedure, giving you a breadth of experience that happens to be progressively difficult to find while in the existence science market.
Building IQVIA’s positions on crucial traits inside the pharma and life sciences industries, with a focus on EMEA.
Specializing in Regulatory Affairs for little molecule and biological merchandise and also Innovative therapies.
GMP compliance is often tough – which rules, which interpretation, in which to begin? We will let you create a GMP compliance roadmap to tutorial you with your way.
We assistance Countless more info firms, together with seventeen of the top 25 world pharmaceutical, biotech, and professional medical device providers, hook up With all the experts they have to have from the ideal workforce product.
Developing with a rich record of creating AI for Health care, IQVIA AI connects the proper information, technology, and skills to handle the special requires of healthcare. It is really what we phone Healthcare-quality AI.
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Regulatory Compliance Associates is greatly regarded throughout the daily life science marketplace and global regulatory organizations for its capacity to aid organizations successfully take care of intricate regulatory troubles, including remediation.
The QA Office is known for policing the controlled processes for the company. They be certain compliance is fulfilled. In order to operate from the QA Division, a person requires thoroughness and attention to depth. There isn't any substitute for QA encounter.
We function to develop procedures and supply options that successfully fulfill our clients' urgent and extensive-phrase world products progress requires.