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Who we are

About Pharmateq

Pharmateq is a pharmaceutical GMP consultancy based in Jagatpur, Ahmedabad. We design compliant facilities from concept to commissioning, upgrade existing plants to Revised Schedule M and WHO-GMP, write the documentation regulators ask for, and train the people who have to live with it.

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Last updated: 14 August 2026

Compliance is not a certificate. It is a habit.

Most consultants hand you a binder and a bill. Six months later the SOPs are out of date, the trained staff have left, and the next inspection finds the same gaps.

Pharmateq works differently. We do the technical work ourselves. We lay out your facility for correct material and personnel flow. We engineer your HVAC, cleanroom, purified water, WFI and clean steam systems. We prepare your URS and detailed engineering packages. We write your QMS, your SOPs, your BMRs, your qualification and validation protocols. We conduct the mock audit that tells you what the regulator will find. And we are physically present when the regulator arrives.

Then, and this is the part most firms skip, we stay. Weekly or monthly site visits. Ongoing training with effectiveness checks. Live documentation updates. For up to five years, if you want us.

Who we serve

  • Oral solid dosage and liquid formulation units
  • Sterile and injectable facilities
  • API and bulk drug manufacturers
  • Cosmetic, nutraceutical and Ayurvedic units
  • Greenfield projects, brownfield expansions, and plants facing a compliance deadline

Questions

The five we are asked most

How long does Revised Schedule M compliance take?
A gap assessment takes 2-4 weeks. Full remediation typically runs 6 to 18 months, depending on how much civil, HVAC and utility work your facility needs. Documentation-only gaps can be closed in 3-4 months.
What does a Schedule M upgrade cost?
Industry estimates for a full MSME facility upgrade commonly fall between Rs 10 and Rs 15 crore, but that figure assumes a complete rebuild. Most plants we assess need considerably less once mandatory items are separated from optional ones. We give you a costed breakdown before you commit to anything.
Do you work outside Gujarat?
Yes. We are based in Ahmedabad and work across India, including Baddi, Indore-Pithampur, Hyderabad and Mumbai. For clients outside Gujarat we typically combine monthly on-site visits with continuous remote documentation support.
Will you be present during the actual inspection?
Yes. Presence and support during customer and regulatory audits is part of our standard engagement.
What is the difference between Schedule M and WHO-GMP?
Revised Schedule M is India statutory GMP requirement under the Drugs and Cosmetics Rules, and mandatory for every licensed manufacturer. WHO-GMP certification is a separate, voluntary certification usually required for export markets. The revised Schedule M was aligned with WHO standards, so a compliant plant is well positioned for WHO-GMP, but they are not the same thing and require separate documentation.

Start here

Find out what your plant actually needs.

A 30-minute call, no charge, no obligation. Tell us your dosage form, your licence status and your deadline. We will tell you honestly whether you have a documentation problem, an engineering problem, or both.

  • A senior consultant on the call, not a salesperson
  • A written summary of what we discussed within 48 hours
  • No proposal until you have seen a gap report
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