Our Experts
IMEX Consultancy Services is backed by a team of seasoned regulatory professionals with decades of hands-on experience across pharmaceuticals, cosmetics, medical devices, food regulations, and clinical research.
Senior Regulatory Affairs Consultant
Drug Manufacturing Licenses · GMP / Schedule M · CDSCO
A seasoned pharmaceutical regulatory professional with over two decades of experience in drug manufacturing licensing, GMP compliance, and CDSCO submissions. Has guided 200+ pharmaceutical units through facility setup, Schedule M compliance, and regulatory inspections across Gujarat, Maharashtra, and Rajasthan.
Areas of Expertise
Cosmetics & Medical Device Regulatory Expert
Cosmetics Rules, 2020 · Medical Devices Rules, 2017 · CDSCO Import
Specialist in cosmetic product licensing and medical device regulatory affairs. Extensive experience in CDSCO import registrations, Cosmetics Rules 2020 compliance, and Class A–D medical device licensing. Has supported domestic and international brands in navigating India's evolving cosmetic and device regulatory landscape.
Areas of Expertise
Food & Nutraceutical Regulatory Advisor
FSSAI · Food Supplements · Health Products
Expert in FSSAI licensing, food supplement regulatory frameworks, and nutraceutical product compliance. Has assisted food manufacturers, importers, and health supplement brands in obtaining FSSAI approvals, product registrations, and compliance documentation across India.
Areas of Expertise
Legal & Enforcement Compliance Specialist
Drugs & Cosmetics Act · NDPS Act · Court Matter Support
A highly experienced regulatory compliance specialist with deep expertise in the Drugs & Cosmetics Act, 1940, NDPS Act, 1985, and enforcement matters. Has provided technical and legal documentation support in regulatory proceedings, NSQ drug investigations, and Risk-Based Inspection preparedness for pharmaceutical companies across India.
Areas of Expertise
Clinical Research & Stability Study Expert
Clinical Trials · GCP · ICH Stability Guidelines · SMO
Clinical research professional with extensive experience in clinical trial management, Site Management Organization (SMO) operations, and stability study design. Specialises in GCP compliance, BA/BE study coordination, pharmacovigilance, and ICH/WHO stability protocols for pharmaceutical and nutraceutical products.
Areas of Expertise
Quality Assurance & Testing Laboratory Consultant
NABL Labs · IP/BP/USP Testing · GMP Quality Systems
Quality assurance expert with a strong background in pharmaceutical testing, NABL-accredited laboratory coordination, and quality management systems. Has supported manufacturers in raw material testing, finished product release, stability studies, and method validation across drug, food, and cosmetic categories.
Areas of Expertise
Our mentors bring decades of combined experience to every client engagement — ensuring your regulatory journey is smooth, compliant, and cost-effective.
Schedule a Free Consultation