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Home
About Us
Core Services
Pharmaceuticals
Pharmaceutical Regulatory Consulting Services
Pharmacovigilance Regulatory Support
Regulatory Affairs Consultation for Life Sciences and MedTech
Regulatory Compliance Consulting, Gap Analysis and Remediation
Regulatory Intelligence
Regulatory Medical Writing Services
Medical Devices
Medical Devices Regulatory Consulting Services
Medical Device Submissions and Medical Device Registrations
MOH Interaction and Regulatory Liaison Support
Regulatory Publishing Services for Medical Devices
Medical Device Labeling Services and Technical Writing Support
Insights
Blogs
Brochure
Case Studies
Press Releases
Contact Us
Insights
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Insights
By Vigilare Biopharma
December 12, 2023
Understanding Good Pharmacovigilance Practices (GVP): Ensuring the Safe Use of
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By Vigilare Biopharma
November 22, 2023
RFDA Registration & Listing of Cosmetic Product Facilities and Products
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By Vigilare Biopharma
October 30, 2023
Biologics: Transforming Cancer Treatment for Improved Safety and Efficacy
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By Vigilare Biopharma
October 6, 2023
Scope of The Safety Specification ICH E2E guideline in Pharmacovigilance
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By Vigilare Biopharma
September 22, 2023
Pharma and Regulatory News Sep 22
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By Vigilare Biopharma
August 28, 2023
Outsourcing Pharmacovigilance to CROs: Benefits, Challenges and Best Practices
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By Vigilare Biopharma
August 16, 2023
How decentralized clinical trials-DCTs are transforming clinical research and patient
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By Vigilare Biopharma
August 8, 2023
FDA Approves Zurzuvae: First Oral Medication for Postpartum Depression (PPD)
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By Vigilare Biopharma
August 1, 2023
Patient Engagement in Pharmacovigilance: Empowering Patients for Safer Healthcare
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