At JD Pharma Services, we are committed to guiding pharmaceutical, biotechnology, and medical device companies through the complex journey of product development, regulatory approval, and post-marketing safety monitoring. With a deep understanding of global regulatory frameworks and a dedication to patient safety, we provide end-to-end solutions in Regulatory Affairs, Pharmacovigilance, and Clinical Research.
Who We Are ?
Founded on the principles of quality, compliance, and scientific excellence, JD Pharma Services brings together a team of experienced professionals with diverse expertise across the life sciences sector. Our mission is to support healthcare innovation by ensuring that every product we work on meets the highest standards of safety, efficacy, and regulatory compliance.
Our Services
Regulatory Affairs
- Dossier preparation and submission (CTD/eCTD)
- Regulatory strategy & gap analysis
- Product lifecycle management & compliance updates
- Global market authorization support
Pharmacovigilance
- Safety data collection, evaluation & reporting
- Signal detection & risk management plans
- Aggregate safety reports (PBRERs, PSURs, DSURs)
- Pharmacovigilance system setup & audits
Clinical Research Support
- Clinical trial documentation & protocol development
- Site & investigator support
- Compliance with GCP and ICH guidelines
- Data management & medical writing
Why Choose Us ?
- Expertise That Delivers: Years of hands-on experience in highly regulated markets.
- Tailored Solutions: Customized approaches for every client and project.
- Global Reach: Understanding of diverse regulatory requirements across regions.
- Quality & Compliance: Unwavering focus on meeting international standards.
Our Commitment
We believe that patient safety and regulatory compliance are not just obligations—they are the foundation of responsible healthcare innovation. Every project we undertake is driven by our promise to deliver accuracy, transparency, and trust.
Dr. Joan D’souza
She/Her
Pharmacovigilance Consultant/FvP/ QPPV/ LCPRA/PRRC/ M.Sc./JD/Medical Reviewer/Medical Devices/ Aggregate Reporter/Lead Auditor/Medical Writer/ No visa required to work in the US or Switzerland
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