Building Lasting Strategic Partnerships based on Trust, Transparency, and a Customer-first Mindset
The Perfect Partner When You Want to Turn Innovation Into Impact
At APCER Life Sciences, we help bring safe and effective therapies to patients worldwide. For nearly two decades, we have partnered with pharmaceutical, biotech, and medical device companies to navigate complex global regulations and turn scientific innovation into real-world impact.
Our teams are 100% healthcare professionals, including a 15% physician pool, delivering deep expertise across the full product lifecycle. From pharmacovigilance and medical information to regulatory affairs, medical writing, and quality assurance, we provide integrated, fit-for-purpose technology powered solutions built to the highest standards.
With a global footprint across North America, the UK, Europe, and Asia, and experience supporting products in 100+ markets, we offer scalable, flexible models tailored to your needs. Trusted by 90+ customers since 2007, APCER is known for regulatory rigor, operational reliability, and consistent quality every time.
At the Heart of APCER is a Clear and Confident Purpose
Vision
Improving health by enabling safe and effective therapies for everyone, everywhere
Mission
Our expertise in medicine, science, and technology powers us to achieve best in class quality, deliver optimal results, and build enduring partnerships founded on trust.
Values
Ethical, Trustworthy, Collaborative, Enterprising, Agile
Real Results. Real Trust.
Real Stories
Sincerely thank you for all the effort, thoroughness and professionalism that went through conducting and reporting on this FDA PADER Gap Analysis as we now embark on our journey towards documentation and process improvement to ensure readiness for an actual inspection.
Director, Drug Safety and Medical Information
Canada-based global pharma
The APCER Pharmacovigilance team demonstrated exceptional collaboration and inspection readiness during FDA PADE Inspection. The accuracy, consistency, and completeness of expedited reports, reconciliations, and aggregate safety documentation clearly reflected strong teamwork and compliance across all deliverables.
VP, Regulatory and Quality
US-based biopharma
With all the transformation and rapid growth happening, having a reliable PV/med info partner like the APCER group has truly been invaluable—it’s made a real difference in helping us navigate the complexities and keep challenges to a minimum.
VP, Medical Affairs
US-based specialty pharma
... the preparation and support for our BPD Type 2a meeting were a strong example of APCER’s commitment and effectiveness and instrumental in keeping us aligned and confident in our regulatory strategy. We have greatly valued the team’s responsiveness, collaborative approach, and sound regulatory judgment.
Chief Medical Officer
A clinical-stage biopharma
Phase 1 completion is an achievement that demonstrates APCER's scalability, flexibility, and operational readiness. It reflects exceptional cross-functional collaboration.
Associate Director, IT Business Partner
Japan-headquartered, global healthcare company
I want to sincerely appreciate all the great work Team APCER has been doing. Their strong attention to detail, agility in handling tasks, and consistent respect for timelines have been truly impressive.
Associate Director, Safety Physician
Japan-headquartered, global healthcare company
Deep gratitude to entire APCER team for their efforts in working hard to complete the cases. While the system outage was well beyond their control, their strong work to make up for the lost time ensured that we're able to maintain compliance.
Associate Director, Pharmacovigilance Operations
US-based biotech
Sincere appreciation for APCER's partnership and dedicated service. The team’s commitment, adaptability, and collaborative approach have been instrumental in supporting our pharmacovigilance operations through both high and low volumes of activity.
Sr.Director, PV Operations-Global Case Management
US-based biotech
I’ve greatly valued APCER’s commitment to excellence. Their contributions have played a key role in helping us uphold our compliance standards and achieve strong performance across key metrics, including timely deviation closure, audit readiness, and quality of deliverables.
Sr. Director PV Ops – Pharmacovigilance Center of Excellence
US-based biotech
