Driving Clinical Success with Trusted Innovation & Expertise.
Backed by 20+ years of success in clinical trials, we’ve built a powerful advantage proprietary technologies, agile processes, and innovative problem-solving—designed to accelerate even the most complex clinical development programs.
FDAMap is now GSA Registered
CLINICAL TRIALS
Clinical trial, site certification and patient recruitment services.
REGULATORY SERVICES
As regulated by the US FDA, EMA and similar agencies
FDA AUDITING
For drug and device manufacturers in FDA audit preparation
QUALITY ASSURANCE
Quality assurance and regulatory GxP compliance services
TRAINING & WORKSHOPS
Customized FDA training programs and one-on- one consultation
Who We Are
FDAMap, a trademark of Brij Strategic Consultations, LLC, is a global network of experts in healthcare, food regulations, business, and public policy. With decades of collective experience, we support professionals, regulators, & government agencies in regulatory submissions, clinical trials, quality assurance, training, and consultation. Our mission is to foster education, compliance, & professional growth through collaborative platforms, ensuring success for both experts & newcomers in the industry.
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A Global CRO & Regulatory Consulting firm specializing in Clinical Trials.
We offer a full spectrum of regulatory, compliance, and clinical study services for drug and device companies governed by the US FDA, EMA, and other international regulatory agencies.
Clinical Trial
We provide a comprehensive range of clinical trial, site certification & patient recruitment services.
Regulatory Services
We provide regulatory consultation & quality assurance services to companies regulated by the US FDA, EMA & similar agencies in other countries.
Project Management
Our qualified project managers & experienced consultants provide regulatory information and quality assurance for successful project outcomes.
FDA Auditing
We help train drug and device manufacturers in FDA audit preparation and conduct mock FDA audit at their premises.
Quality Assurance
We provide comprehensive range of quality assurance and regulatory CxP compliance services to the pharmaceutical, medical device, biotechnology, dietary supplement and other FDA-regulated industries
Why Choose FDAMap?
FDAMap is a global CRO helping you get the most out of your investment in R&D with our group of regulatory and clinical trial experts.
- Global CRO with Regulatory Expertise
- End-to-End Clinical & Regulatory Support
- US FDA Compliance
- Pharmacovigilance & Clinical Trials
- Accelerated Product Development Strategy
- US Authorized Agent Services:
- European Medicines Agency (EMA) Compliance
- Proven Quality Assurance & Control Framework
Latest FDA Purán Blogs
Visual Recap: Past Seminars
For any information on the training agenda and logistics, please call +1 410-501-5777 or email: info@fdamap.com
