About Zoop

ZOOP Technical Service (sz) Co., Ltd. (Zoop), established in 2010, is headquartered in the vibrant and innovative city of Shenzhen. As a professional product regulatory compliance consulting firm, Zoop specializes in researching product compliance and market access regulations worldwide. Over 80% of our team members come from leading domestic and international testing organizations and large-scale manufacturers, with all technical team members holding backgrounds in biology, chemistry, pharmaceuticals, cosmetics, or related fields. Our regulatory research team closely monitors regulatory updates and maintains active communication with authorities to ensure timely awareness of changes and swift responses to client needs.

Since 2010, Zoop has focused on regulatory research, product registration and filing, and quality system enhancement, accumulating extensive experience in domestic and imported cosmetics, disinfectant products, and medical device registration and filing. With professional and meticulous high-quality services, we have earned the trust and recognition of premium domestic and international brands and traders, successfully completing over 100,000 product filings and registrations.

We believe that knowledge, experience, and a responsible approach are the cornerstones of our continuous growth and success. Today, Zoop is recognized as one of the most professional and trusted product compliance consulting firms in the industry.

Service Overview

Cosmetics

•  Domestic General Cosmetics Filing Services

•  Domestic Special Cosmetics Registration Services

•  Imported General Cosmetics Filing Services

•  Imported Special Cosmetics Registration Services

•  Cosmetics Manufacturing License Application Services

•  Cosmetics Safety Assessment Services

Cosmetics Export

•  USA: MoCRA OTC

•  ASEAN (Singapore, Malaysia, Thailand, Vietnam, Indonesia, Philippines): TFDA, BPOM

•  EU: CPNP

•  UK: SCPN

•  Australia: AICIS, ACCC, TGA

New Raw Materials

•  New Raw Materials Registration and Filing Services

•  New Raw Materials Safety Assessment Services

•  New Raw Materials Declaration Gap Analysis and Technical Documentation Compilation

•  Physicochemical and Toxicological Testing-Related Services

Disinfectant Products

•  Domestic and Imported Disinfectant Product Filing Services

•  Disinfectant Product Technical Standard Documents Compilation

•  Antibacterial Products Registration Services

•  New Disinfectant Product Registration Services

•  Disinfectant Product Manufacturing License Application Services

•  Disinfectant Device and Preparations Testing Services

Quality Systems

•  GMP Quality System Setup and Guidance

•  Adverse Reaction and Recall System Training and Setup Guidance

•  Regulatory-Based System Pre-Audit Services (Mock Inspections)

•  US OTC Product CGMP System Guidance

•  Process Validation and 3Q Validation Services

Others

•  Domestic Class I & II Medical Device Registration

•  Imported Class I & II Medical Device Registration

•  Medical Device Qualification Filing and Licesing

•  Cosmetics Testing Services

•  Regulatory Training

Registration method