REGULATORY AFFAIRS FOR PHARMACEUTICALS
Get your pharmaceuticals to market efficiently and keep them there with confidence.
REGULATORY AFFAIRS FOR PHARMACEUTICALS
Get your pharmaceuticals to market efficiently and keep them there with confidence.
SUPPORT YOUR REGULATORY PROJECTS
You have a drug that needs to go to market – and stay there. But a lot can go wrong between product development and securing approval from regulatory agencies. Without the right strategy and people to execute, you’re limiting future expansion. Our Regulatory Affairs professionals are resourced and backed by a team of industry experts.
CRITICAL REGULATORY SUBMISSIONS DEMAND SUCCESSFUL OUTCOMES
Get your submissions approved faster with fewer rounds of questions and revisions.
CRITICAL REGULATORY SUBMISSIONS DEMAND SUCCESSFUL OUTCOMES
Get your submissions approved faster with fewer rounds of questions and revisions.
WHY FLEXPRO?
Our team of degreed, highly trained, specialized life sciences professionals integrates with yours to provide immediate, valuable contributions to your existing pharmaceutical operations. With our team, you don't have to settle. Get the results you need.
GAIN A TRUE REGULATORY AFFAIRS PARTNER
We work with you to develop project strategy and enhance your team with experienced pharmaceutical professionals who support your objective. Our primary interest is in the successful execution of your project.
REGULATORY AFFAIRS PROFESSIONALS, JUST LIKE YOU
Our leadership has held top positions at life sciences companies. We have curated a team of specialized Regulatory Affairs professionals to bring the expertise and industry knowledge required to produce results.
OUTCOME-DRIVEN PARTNERSHIP
Through training, mentorship, and ongoing professional development, our exceptional Regulatory Affairs professionals are qualified, experienced, and equipped to achieve success.
JOB OPENINGS
Join our team of inspired professionals who engage in challenging and diverse programs that positively impact patients’ lives.
Packaging Engineer
The FlexPro Group, is seeking to hire a Packaging Engineer to join our team that will work with our client partners to ensure the company's products and processes meet established standards.
CER Writer
Network Partners is seeking to hire an experienced Medical Writer to our team that will be responsible for writing and developing Clinical Evaluation Reports (CERs) under the MEDDEV 2.7/1 revision 4 and EU MDR guidelines for our client partners.
Principal Regulatory Affairs Consultant
Network Partners is seeking to hire a Principal Regulatory Affairs Consultant to our team that will work with our client partners to ensure that their products and processes meet established regulatory standards by identifying shortfalls, developing corrective measures, and implementing regulatory systems.
EXPLORE OUR OTHER PHARMACEUTICAL SOLUTIONS
Whatever your project needs, the team at FlexPro offers valuable industry experience, professional resources, and dedicated support to handle all your pharmaceutical needs from strategy to execution.
