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CDSCO & DCA approved analytical testing laboratory

Mediviz Pharma

Microbiology testing laboratory in Visakhapatnam.

The Mediviz Unit 1 laboratory in Visakhapatnam (Vizag), Andhra Pradesh, provides microbiology and selected analytical testing for pharmaceutical, biotechnology, and allied-sector requirements.

Scientist using a microscope in an analytical laboratory

NABL-accredited microbiology testing for pharma and allied sectors.

Our microbiology testing laboratory is operated by experienced microbiologists working across routine analysis, advanced techniques, research microbiology, and specialised testing.

The facility and its procedures are structured around cGMP expectations, cleanroom controls, documented operating practices, and quality review. Testing support covers water, cleanrooms, APIs, raw materials, packaging materials, pharmaceutical formulations, equipment holding studies, and validation programmes.

“The aim is straightforward: useful results, communicated clearly, delivered with the discipline regulated teams require.”

Exterior view of the Mediviz microbiology laboratory, Unit 1
  • CDSCO · DCA (A.P.): Approved analytical testing laboratory
  • ISO/IEC 17025:2017: NABL accredited laboratory

A focused analytical service portfolio.

Select a service area to begin the discussion; the Mediviz team can confirm method, sample, documentation, and turnaround requirements.

Testing support from Vizag for regulated laboratories.

  • Where is the Mediviz microbiology testing laboratory?

    Unit 1 is located at Lankelapalem in Visakhapatnam (Vizag), Andhra Pradesh. The laboratory supports enquiries from pharmaceutical and allied-sector organisations across India.

  • Does Mediviz test compressed air and nitrogen gas?

    Yes. The listed scope includes chemical and physical parameters, purity by GC, and microbiological testing for compressed air and nitrogen.

  • What pharmaceutical materials can the laboratory support?

    The listed service scope includes water, cleanrooms, APIs, raw materials, packaging materials, pharmaceutical formulations, equipment holding studies, and validation programmes.

  • Which cleanroom monitoring methods are listed?

    The service portfolio includes settle plates, active air sampling, RODAC or contact plates, and surface swabs.

Testing coverage

Materials and environments listed in the laboratory scope.

  1. 01

    Controlled environments

    Water, cleanrooms, environmental monitoring, equipment holding studies, and disinfectant validation.

  2. 02

    Pharma materials

    APIs, raw materials, packaging materials, and pharmaceutical formulations.

  3. 03

    Utilities

    Compressed air and nitrogen gas testing for chemical, physical, and microbiological parameters.

Have a sample or method to discuss?

Share the sample type, standard, specification, and expected timeline for a technical review.