Since 1996 the Pharm Assist team has been dedicated to provide reliable and committed service in the strictly regulated fields such as regulatory affairs, medical writing, pharmacovigilance and quality assurance. We have successfully collaborated with more than 200 companies in the pharmaceutical and MedTech industry.
At Pharm Assist you will be designated a contact person to focus on the specific regulatory needs of your business. Our consultants have different backgrounds and experience but all strive to bring success to your project by providing solutions including one or more of our service areas. Pharm Assist provides both staff for outsourcing or in-house consulting, part time or on demand.
Regulatory decisions have a direct impact on business outcomes. Our main focus is to give companies in the pharmaceutical and medical device industry the ability to reach their visions. Pharm Assist acts as partner in product development, authoring and compilation of dossier for submission, regulatory procedures and maintenance, medical writing, pharmacovigilance and wholesale quality.
Through a network of qualified partners, we can provide support throughout Europe.