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Domestic and Foreign Drug Marketing License Registration

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What We Do
  • Medical and Regulatory Affair
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  • Domestic and Foreign Drug Marketing License Registration

 

OUR SERVICE04

We have excellent professionals,
Help you apply for a drug license based on your needs.

If you're looking for a regulatory team with a wealth of experience in registering drugs and medical devices, ClinHope has got you covered.
Our team is well-versed in navigating the complex regulatory landscape, ensuring that your product meets all the requirements for market approval.
 

 
Our organization excels in clinical research and is widely recognized for our expertise and innovative approach to scientific endeavors. With a rigorous and state-of-the-art methodology, we ensure reliability and accuracy in all our projects. Our reputation is built on our attention to detail, ethical practices, and highly skilled team, which consistently delivers comprehensive results. Additionally, our adaptable and collaborative nature, combined with a client-focused and results-driven mindset, has established us as a trustworthy and pioneering force in clinical research. We use our extensive experience to facilitate product registration by maintaining open communication channels with regulatory agencies and streamlining the review process.

 
Our Domestic and Foreign Drug Marketing License Registration Services:
  • Foreign pharmaceutical factory (PMF) application
  • Application for Foreign API Factory (DMF)
  • ECTD folder review
  • Drug safety monitoring after marketing

ClinHope Consulting Co., Ltd.

12F., No. 144, Sec. 3, Minquan E. Rd., Songshan Dist., Taipei City 105401, Taiwan (R.O.C.)
info@clinhope.com
+886-2-2835-3685
 @424rzdfm
 clinhopeconsulting
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