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U.S. Medical Device Registration Requirements and Process
U.S. Medical Device PMA Application Guidelines and Key Points
FDA Breakthrough Device Program and Progress
How to Apply for a UDI and Enter it into the GUDID Database
FDA Investigational Device Exemption (IDE) Application Process
FDA Small Business Qualification Application
De Novo Request Helps Bring Low and Medium Risk Devices to Market
Development and Strategy for In Vitro Companion Diagnostic Devices
MDR Device Classification and Regulatory Guidelines
FDA Special 510(k) Program Application Requirements and Review Points
Key Strategies for Medical Device PMA Applications
Medical Device Regulations in Australia and New Zealand
7 Steps to Comply with FDA's QMSR
FDA Corrective and Preventive Actions (CAPA) Procedure Guidelines
14 Questions To Self-Check Medical Device Regulation (MDR) Compliance

Canadian API Type-Ⅰ MF Guidelines
Global Standards for Pharmaceutical Water Classification
FDA Orphan Drug Designation Process
How to Design a Clinical Trial Protocol
EU ASMF Regulations Guidelines
EU CEP Certificate Application
China Drug Registration Guidelines
U.S. DMF eCTD Format Details
NMPA IND Application
How Pharmaceutical Companies Choose Qualified Suppliers
FDA Requirements for Diversity of Subjects in Clinical Trials
How Can Real-World Data (RWD) Be Used in FDA Drug Registration Applications
FDA Releases Elsa AI Tool to Improve Operational Efficiency
Overview of Japan's Pharmaceutical Regulatory Framework
EDQM Releases New Edition of How to Read CEP
Essentials of US IND Application
NMPA Generic Drug Registration Guidelines
7 Common Questions About IND Application

U.S. Cosmetics Registration Guidelines
How Can Cosmetics Be Sold on Amazon US
NMPA Import General Cosmetics Filling Process
UK Cosmetics Compliance Requirements and Procedures
Registration Process and Requirements for Japanese Imported Quasi-drugs
Canadian Cosmetics Notification Guidelines
Analysis of the Regulatory System for Imported Cosmetics in South Korea

FDA Food Color Additives Application
Registration Process for Foods for Special Medical Purposes (FSMP) in China

Four Steps to Complete U.S. EPA Chemical Registration

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