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Home
About Us
Solutions
Functional Service Provision
Patient Recruitment
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Marketing and Customer Experience
Services
Medical Affairs
Material Review and Compliance
Medical Information Management
Medical Communication and Publications
Medical Science Liaisons
Medical Excellence
Health Economics and Outcomes Research
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PDE Reports(Permitted Daily Exposure)
OEL & API categorization
Nitrosamine Impurities
(Q)SAR Assessment
Impurities And Risk Analysis
Clinical Research & Generic Development
Early Phase
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GENERIC DEVELOPMENT
Bioanalytical Services
Bioavailability & Bioequivalence
Regulatory Affairs
HEOR Health Economics and Outcomes Research
Data Sciences
Clinical Informatics
NGS Data Analysis
Variant Interpretation Services
Content Enrichment Services
Pharma Competitive Insights
Medical Writings
Pharmacovigilence & Safety
Safety Industry Networks
End-to-End Pharmacovigilance Services
Safety Reports
Regulatory Compliance, Gap Analysis & Remediation
QPPV Support
Industries We Serve
Medical Devices
Medical Devices Classification
Quality Management System Compliance
Clinical Evaluation Report – CER
Clinical Consultation
Market Compliance Consulting
Medical Devices Regulation (MDR)
In Vitro Diagnostic Regulation (IVDR)
Performance Evaluation Report (PER)
513G
510K
Pharmaceutical
Biologics
Cosmetics
Review and Product Classification
Cosmetic Product Safety reports (CPSR)
Cosmetics Claims and Substantiation Services
Cosmetic Labeling Review
Product Information / Technical File Compilation (PIF)
Go-to-Market Services and regulatory Intelligence
Research & Development Solutions
Food Supplements & Nutraceuticals
Regulatory overview and product classification
Food Ingredients and Additives
Claims and Substantiation of claims
Labeling Review
Product Registration/Notification
Go-to-Market Services
Research and Development
Chemicals
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Reach
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The Count- down has started for EUROPEAN UNION Medical Devices Regulation ( MDR) – Decode the Key Factors to be Considered as per EU MDR
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FDA Extends Compliance Dates for Class I & Unclassified Devices
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Medical Devices Labeling Checklist for EU MDR Compliance
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