Accelerate Your Path to Market Approval
Your Trusted Partner for Clinical Development and Beyond
Successful clinical development requires more than just a vendor, you need a friend, philosopher, and guide with significant experience. With nearly 2 decades of experience in clinical development, APCER is your one-stop support from clinical trials to post-approval. We deliver comprehensive solutions in pharmacovigilance, regulatory affairs, medical writing, medical information, and quality assurance. Our integrated ISO Certification and impeccable track record ensure the highest quality outcomes for your molecule. Backed by deep expertise across multiple therapeutic areas, and 100% HCP delivery teams, we have enabled companies such as yours to scale seamlessly both in size and markets. For APCER, your success is our goal.
End-To-End Coverage to Meet All Your Clinical Phase Needs
IND/ CTA
Clinical Trials
NDA/BLA/MAA
Product Approval and Launch
Case Studies
Get your trial back on track with smart medical monitoring that combines local expertise with global efficiency
Partner with us - Tap into APCER'S ready-to-go local experts who speak your regulators' language
Get your drug approvals fast-tracked with expert submission management
Keep your new market entries on schedule with APCER!
Transform challenges into compliance with a unified global pharmacovigilance system
Get expert PSMF management that keeps you inspection-ready and compliant
Meet tight deadlines with confidence using expert medical writers
Go live in record time with a trusted partner who will own the process end to end
Turn uncertainty into confidence with experts who understand the Regulators expectations
Streamline Your Path to Market with APCER
Your Trusted Guide: We partner you through every step of clinical development and approvals.
Scalable Solutions: Our services grow with your trials, ensuring smooth safety management worldwide.
Ownership of Outcomes: We take responsibility for outcomes of our services, so that you can focus on your path to approval
Proven Expertise: Decades of experience and a global footprint make us a reliable partner.
Quality You Can Count On: ISO certified processes and a robust Quality Management System that ensure excellence.
One-Stop Solution: Pharmacovigilance, medical writing, and regulatory services—all under one roof.
Expert Teams: 100% healthcare professional teams with deep and wide therapeutic are expertise.