Our growing team of 50+ Professionals with a mixed blend of GxP, Regulatory & Engineering domain continuously provide critical support services to Global Pharmaceutical, Biotechnology, Nutraceuticals, Veterinary and Medical Device clients across the globe supported by regional expertise. Our professionals have a wealth of knowledge in QA, QC, Microbiology, API, OSD, Parenteral, Topical, Inhalation, Biologics, Oncology, Medical Devices, GCP, Regulatory, CSV, R&D, PV, and Projects & Engineering.

We have conducted projects in various countries worldwide and has assisted clients globally, ranging from top pharmaceutical companies to one product start-ups.

OUR SERVICES

Our core capabilities and expertise are in the provision of expert, independent Quality Assurance (QA) and Quality Management System (QMS) auditing and consulting, worldwide. Our services include all aspects of:

  • PLANT SET UP AND TURN KEY PROJECTS
  • FDA SERVICES
  • ANALYTICAL DEVELOPMENT
  • API / INTERMEDIATE DEVELOPMENT
  • FORMULATION DEVELOPMENT
  • DOSSIER & DMF MANAGEMENT
  • GOOD MANUFACTURING PRACTICE (GMP)
  • GOOD CLINICAL PRACTICE (GCP)
  • GOOD LABORATORY PRACTICE (GLP)
  • GOOD CLINICAL LABORATORY PRACTICE (GCLP)
  • GOOD PHARMACOVIGILANCE PRACTICE (GVP)
  • CONTRACT MANUFACTURING/OUTSOURCING
  • QUALITY MANAGEMENT SYSTEMS (QMS) CONSULTING
  • QUALITY INVESTIGATION
  • SOP DEVELOPMENT
  • REGULATORY AFFAIRS
  • MARKETING AUTHORIZATION HOLDER
  • QP/RP/RPI SERVICES
  • QPPV SERVICES
  • EUROPEAN BATCH TESTING & CERTIFICATION
  • AUDIT SERVICES
  • VALIDATION SERVICES
  • GAP ANALYSIS
  • DUE – DILIGENCE
  • BUSINESS DEVELOPMENT SERVICES
  • COMPUTER SYSTEMS COMPLIANCE (CSC) & VALIDATION
  • HR CONSULTING
  • TRAINING

PHARMACEUTICALS

    MEDICAL DEVICES

    • Regulatory Consulting for Medical Devices
    • European Authorized Representative
    • UK Responsible person
    • Regulatory & Technical Document writing
    • Regulatory support for CE marking
    • Clinical trials support in Europe
    • Marketing support in Europe
    • Reimbursement support
    • Quality Management Consulting for Medical Devices
    • Global Product Registration for Medical Devices
    • Market Entry and Market Research Analysis for Medical Devices
    • Medical Devices Training Courses
    • ISO 13485 : 2016 Certification

      United Kingdom:

      20-22, Wenlock Road,
      London, N17GU, England, UK
      T: +44 (0) 20 70976606
      M: +44 (0) 7944 509 807
      E: info.uk@ntherapeutics.uk

      Germany:

      Ebracher Weg 16,
      91056 Erlangen
      Germany
      E: info.germany@ntherapeutics.uk

      South Korea:

      1008-2, 99 Centum dong-ro,
      Haeundae-gu,
      Busan,
      Republic of Korea
      E: info.skorea@ntherapeutics.uk

      India:

      D.No-1-1-336/19, VIVEK NAGAR
      HYDERABAD - 500020
      Telangana – India
      M : +91 (0) 9848 722 266 /
      +91 (0) 7013 380 075
      E: info.india@ntherapeutics.uk

      Uganda:

      Plot 36, Bukoto Cresent Road, Naguru,
      Kampala, P.O Box 30650
      Uganda
      E: info.uganda@ntherapeutics.uk

      Russia:

      Russian Federation
      H.20, Ternovaya Street
      Troitsk, Moscow- 108842
      E: info.russia@ntherapeutics.uk

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