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Pharma Regulatory Service

Service Provider of a wide range of services which include Pharma Regulatory Services, CTD/ACTD/Country-specific Dossier Services, Pharma Registration Services, Standard Operating Procedure (SOP) Services, Pharmaceutical Development Report Service and WHO GMP Certification Service.

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Being a highly effective, lean and fast-moving organization, we are highly instrumental in providing Pharma Regulatory Services. These regulatory services provide CTD submissions (for US, EU, CA, CH, JP, GCC and S. Africa Markets), Non-eCTD submissions (NeeS), paper CTD submissions, CTA (Clinical Trial Application), IMPD (Investigational Medicinal Product Dossier), eCopy (Publishing of PMA, 510(K) and IDE) etc. By our adroit professionals, we provide these regulatory services in the best possible manner.

Regulatory Submission Services for:

  • eCTD Submissions (for US, EU, CA, CH, JP, GCC and S.Africa Markets)
  • Non-eCTD Submissions (NeeS)
  • Paper CTD Submissions
  • CTA (Clinical Trial Application)
  • IMPD (Investigational Medicinal Product Dossier)
  • eCopy (Publishing of PMA, 510(K) and IDE)
  • VNeeS (Veterinary NeeS)

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We are the dynamic, business-oriented organization, ranking among the utmost entities engaged in providing Dossier Services. Provided services are imparted professionally to meet utmost clients’ satisfaction. Our accomplished professionals carry out these services as per the set industry norms and guidelines. Offered services are widely demanded in the market, owing to their superb features like hassle free management, 100% quality assurance, promptness and client-centric approach.

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