Home
About Us
Company Profile
Your trustworthy global compliance consulting service organization
Global Self-operated Matrix
WISELINK GROUP A total of 16 wholly-owned subsidiaries have been established worldwide.
Expert Teams
Meet the team behind our trusted solutions
Join Us
Attracting Talents and Gathering Elites, Guiding Careers for the Future.
Service
Medical Device
Health Food
Cosmetics
Foods
Value-added
Europe
EU(CE)
EU(CE)
ES(AEMPS)
ES(AEMPS)
UK(UKCA)
UK(UKCA)
CH(SWISSMEDIC)
CH(SWISSMEDIC)
IT(AIFA)
IT(AIFA)
SRB(ALIMS)
SRB(ALIMS)
Asia-Pacific
AU(TGA)
AU(TGA)
NZ(MEDSAFE)
NZ(MEDSAFE)
JP(PMDA)
JP(PMDA)
KP(MFDS)
KP(MFDS)
CN(NMPA)
CN(NMPA)
CN HK(MDACS)
CN HK(MDACS)
CN TW(TFDA)
CN TW(TFDA)
IN(CDSCO)
IN(CDSCO)
BD(DGDA)
BD(DGDA)
UZ(MOH)
UZ(MOH)
PK(DRAP)
PK(DRAP)
KZ(FMXM)
KZ(FMXM)
North America
US(FDA)
US(FDA)
US(DMF)
US(DMF)
CA(HC)
CA(HC)
MX(COFEPRIS)
MX(COFEPRIS)
Middle East
SA(SFDA)
SA(SFDA)
EG(EDA)
EG(EDA)
UAE(MOHAP)
UAE(MOHAP)
TR(TITCK)
TR(TITCK)
Africa
ZA(SAFHRA)
ZA(SAFHRA)
ET(EFDA)
ET(EFDA)
NG(NAFDAC)
NG(NAFDAC)
KEN(PPB)
KEN(PPB)
Southeast Asia
SG(HSA)
SG(HSA)
MY(MDA)
MY(MDA)
VN(MOH)
VN(MOH)
ID(MOH)
ID(MOH)
TH(TFDA)
TH(TFDA)
PH(PFDA)
PH(PFDA)
South America
BR(ANVISA)
BR(ANVISA)
PE(DIGEMID)
PE(DIGEMID)
CO(INVIMA)
CO(INVIMA)
AR(ANMAT)
AR(ANMAT)
EC(ARCSA)
EC(ARCSA)
CL(ANDID)
CL(ANDID)
Asia-Pacific
TW(TFDA)
TW(TFDA)
AU(TGA)
AU(TGA)
North America
US(FDA)
US(FDA)
CA(NNHPD)
CA(NNHPD)
Southeast Asia
MY(NPRA)
MY(NPRA)
PH(PFDA)
PH(PFDA)
SG(HSA)
SG(HSA)
TH(TFDA)
TH(TFDA)
Europe
UK(SCPN)
UK(SCPN)
EU(CPNP)
EU(CPNP)
Asia-Pacific
NZ(EPA)
NZ(EPA)
TW(TFDA)
TW(TFDA)
CN(NMPA)
CN(NMPA)
AU(TGA)
AU(TGA)
JP(PMDA)
JP(PMDA)
North America
CN(CNF)
CN(CNF)
US(FDA)
US(FDA)
Southeast Asia
SG(HSA)
SG(HSA)
MY(MDA)
MY(MDA)
PH(PFDA)
PH(PFDA)
VM(MOH)
VM(MOH)
ID(BPOM)
ID(BPOM)
TH(TFDA)
TH(TFDA)
South America
BR(ANVISA)
BR(ANVISA)
Asia-Pacific
CN TW(TFDA)
CN TW(TFDA)
AU(FSANZ)
AU(FSANZ)
North America
CA(CFIA)
CA(CFIA)
US(FDA)
US(FDA)
Southeast Asia
MY(FSQD)
MY(FSQD)
PH(PFDA)
PH(PFDA)
SG(SFA)
SG(SFA)
TH pet food
TH pet food
TH(TFDA)
TH(TFDA)
Clinical Trial
Overseas Clinical Trial Services Australian Clinical Trial Services IVD Clinical Trial Services Clinical Trials
System Guidance
Brazil BGMP MDSAP ISO 13485
Other Services
Apostille Certification Free Sales Certificate Professional Translation Agent Services
Successful Cases
News Center
EN
English
English
Chinese
Chinese
Home > News Center
Global Regulatory Tracking
With timeliness, accuracy and practicality at its core, WISELINK offers regulatory updates, interpretations and trend analysis to help businesses navigate global compliance and drive global growth.
  • Lowest Official Fees! One Registration Certificate for Multiple Importers! CMEF Latin America Open Class – Peru Session
    Lowest Official Fees! One Registration Certificate for Multiple Importers! CMEF Latin America Open Class – Peru Session
    View More
    2026-10-30
  • Can You Secure Mexican Registration Quickly with FDA/CE Approval? Which Countries Are Recognized Reference Jurisdictions? CMEF Latin America Open Class – Mexico Session
    Can You Secure Mexican Registration Quickly with FDA/CE Approval? Which Countries Are Recognized Reference Jurisdictions? CMEF Latin America Open Class – Mexico Session
    View More
    2026-10-29
  • Automatic Registration Does Not Mean Easy Approval! High-Risk Registration Only Has One Supplementary Chance! CMEF Latin America Open Class: Colombia Chapter
    Automatic Registration Does Not Mean Easy Approval! High-Risk Registration Only Has One Supplementary Chance! CMEF Latin America Open Class: Colombia Chapter
    View More
    2026-10-28
  • What Should You Watch Out for in Japan High-Risk Registration? Do You Need Clinical Trials? CMEF Open Class Highlights
    What Should You Watch Out for in Japan High-Risk Registration? Do You Need Clinical Trials? CMEF Open Class Highlights
    View More
    2026-10-27
  • KGMP: On-site Inspection or Document Review? CMEF Open Class Exclusive Insights
    KGMP: On-site Inspection or Document Review? CMEF Open Class Exclusive Insights
    View More
    2026-10-26
  • UK Officially Confirms Indefinite Recognition of CE-Marked Medical Devices: Dual Pathways of UKCA and CE Run in Parallel
    UK Officially Confirms Indefinite Recognition of CE-Marked Medical Devices: Dual Pathways of UKCA and CE Run in Parallel
    View More
    2026-10-23
  • FDA PCCP In-Depth Interpretation: The Fast Track for Iterative Updates of AI Medical Devices
    FDA PCCP In-Depth Interpretation: The Fast Track for Iterative Updates of AI Medical Devices
    View More
    2026-10-22
  • Global Fetal & Neonatal Device Market Analysis: Which Segment Should Chinese Medical Device Manufacturers Target for Overseas Expansion
    Global Fetal & Neonatal Device Market Analysis: Which Segment Should Chinese Medical Device Manufacturers Target for Overseas Expansion
    View More
    2026-10-21
  • Countdown! Philippines PFDA Medical Device Registration Price Increase Window Closes on November 20
    Countdown! Philippines PFDA Medical Device Registration Price Increase Window Closes on November 20
    View More
    2026-10-20
  • Russia Plans to Extend Validity of Medical Device Clinical Trial Registry Rules Until End of 2028
    Russia Plans to Extend Validity of Medical Device Clinical Trial Registry Rules Until End of 2028
    View More
    2026-10-19
  • FDA Fiscal Year 2027 User Fee Rates Officially Take Effect!
    FDA Fiscal Year 2027 User Fee Rates Officially Take Effect!
    View More
    2026-10-16
  • Can medical device system accessories be sold separately in Latin America?
    Can medical device system accessories be sold separately in Latin America?
    View More
    2026-10-15
    • 12345678
    Contact Us
    Fill Form
    Whether you need more information or wish to cooperate with us, we will guide you through every step of the regulatory process. Subscribe to our newsletter for the latest global regulatory updates.