About Bosker Medico

Bosker Medico Services - Global Pharmacovigilance & Regulatory Sentinel

Bosker Medico Services: A Specialized Sentinel in Global Pharmacovigilance & Regulatory Compliance

Bosker Medico Services is far more than a traditional CRO; we are a dedicated technical extension for global pharmaceutical and biotech leaders who refuse to compromise on patient safety.

In an era where Pharmacovigilance is the cornerstone of market longevity and data integrity is the only currency, we provide the specialized rigor required to navigate the high-stakes journey from clinical trials to post-market surveillance.

We serve as the bridge between complex safety signals and global regulatory approval. By integrating deep-tier Drug Safety expertise with clinical precision, we ensure that your therapies are backed by audit-ready data. Headquartered in Ahmedabad, India, we deliver a "Zero-Critical-Observation" approach for US-FDA, EMA, and MHRA inspections.

Our Four Core Centers of Excellence

Delivering specialized oversight and maximum reach through integrated scientific rigor.

1. Global PV & Drug Safety

The Sentinel of Patient Safety. End-to-end oversight and GVP-compliant assets (PBRER, PSUR, RMPs) meeting US-FDA, EMA, and MHRA expectations.
2. Regulatory Medical Writing

The Voice of Your Science. Expert authoring of eCTD safety modules and high-fidelity scientific narratives for rapid health authority approval.
3. Clinical Research & CSV

The Blueprint of Data Integrity. Securing the digital foundation via 21 CFR Part 11, GAMP 5, and ALCOA+ principles for audit-ready data.
4. Specialized SMO

The Engine of Accelerated Trials. Strategic site management in Oncology and Cardiology, delivering rapid recruitment and high-fidelity data.