TENVIK ATOMICA GLOBAL SOLUTIONS
TENVIK ATOMICA GLOBAL SOLUTIONS
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    • Company Profile
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    • Regulatory & Compliance
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    • Pharma & Natural Products
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    • QC chemicals & apparatus
  • Services
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    • Training
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    • Resource center
  • More
    • Home
    • About Us
      • Company Profile
      • Our Services
    • Consultancy
      • Turnkey Pharma Solutions
      • Regulatory & Compliance
    • Trade & Export
      • Pharma & Natural Products
      • Spare parts
      • QC chemicals & apparatus
    • Services
      • Third party audit
      • Training
      • Quality
    • Solutions
      • Global Market Entry
      • Branding & Packaging Solu
    • Resources
      • Blogs & Articles
      • Resource center
  • Home
  • About Us
    • Company Profile
    • Our Services
  • Consultancy
    • Turnkey Pharma Solutions
    • Regulatory & Compliance
  • Trade & Export
    • Pharma & Natural Products
    • Spare parts
    • QC chemicals & apparatus
  • Services
    • Third party audit
    • Training
    • Quality
  • Solutions
    • Global Market Entry
    • Branding & Packaging Solu
  • Resources
    • Blogs & Articles
    • Resource center

Pharmaceutical Training Services

Good Manufacturing Practices (GMP / cGMP)

  • Principles of GMP & cGMP
     
  • Facility & equipment hygiene
     
  • Documentation practices (BMR, SOP, Logbooks)
     
  • Data integrity & ALCOA+ compliance

Quality Management & Compliance

  • Quality Risk Management (ICH Q9)
     
  • CAPA (Corrective & Preventive Actions)
     
  • Deviation & change control handling
     
  • Internal & external audit readiness

Laboratory & QC/QA Training

  • GLP (Good Laboratory Practices)
     
  • Analytical method validation & calibration
     
  • Stability studies & documentation
     
  • Handling out-of-specification (OOS) & out-of-trend (OOT) results

Production & Operations Training

  • Equipment qualification & validation
     
  • Process validation (ICH Q8/Q10 principles)
     
  • Batch manufacturing process training
     
  • Cleaning & cross-contamination prevention

Regulatory & Documentation Training

  • Regulatory submission requirements (USFDA, EMA, CDSCO)
     
  • Technical dossiers & DMF preparation
     
  • Audit inspection handling (mock audits, FDA/WHO audit preparedness)
     
  • Serialization & traceability compliance

Specialized Training

  • EHS (Environment, Health & Safety) compliance
     
  • Pharmacovigilance & adverse drug reporting
     
  • Supply chain & GDP (Good Distribution Practices)
     
  • Soft skills for pharma professionals (leadership, communication, teamwork)

PHARMACEUTICAL TRAINING SERVICES

Training Formats

✔ On-site training at client facilities
✔ Virtual classroom sessions
✔ Workshops & seminars
✔ Customized training modules based on client needs 

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