GMP
GMP support focused on production discipline, not paperwork for its own sake.
We assess your production facility and processes against applicable GMP requirements, help close gaps, and prepare your documentation for certification.
What is GMP?
Good Manufacturing Practices (GMP) are a set of guidelines covering facility design, hygiene, equipment, processes and quality controls needed to consistently produce safe, quality products — most commonly applied in food, pharmaceutical, cosmetic and nutraceutical manufacturing.
GMP requirements vary somewhat by sector and target market — a food manufacturer, a cosmetics unit and a nutraceutical facility are assessed against related but distinct expectations. A closely related practice, Good Laboratory Practice (GLP), applies specifically to testing and research laboratories rather than production facilities.
Certification or attestation of GMP compliance is granted by the relevant accredited certification body or, for regulated pharmaceutical products, by the applicable drug regulatory authority. Gurur Consultancy helps assess your facility and processes, close documented gaps, and prepare for that assessment.
Why this matters for your business
Who typically needs GMP?
Applicability varies by business — here’s who this usually applies to.
- Food, beverage and nutraceutical manufacturers
- Cosmetic and personal-care product manufacturers
- Contract manufacturers producing on behalf of other brands
- Exporters whose target markets expect GMP-compliant sourcing
Eligibility & requirements
- Applicable to manufacturing facilities in the sectors above; specific requirements depend on product category and target market
- Pharmaceutical manufacturing carries additional statutory drug-licensing requirements beyond GMP certification, which we can advise on separately
Documents & information
Commonly required documents may include:
How we take this forward
- 01
Facility Assessment
We review your facility, equipment and processes against applicable GMP requirements.
- 02
Gap Identification
Hygiene, process-control and documentation gaps are identified.
- 03
Documentation
We help build the SOPs, batch records and quality-control procedures GMP expects.
- 04
Implementation
Corrective actions and new procedures are put into practice.
- 05
Certification/Assessment Audit
The relevant accredited certification body or regulatory authority audits the facility.
- 06
Certification Issued
GMP certification or attestation is issued, subject to periodic renewal or surveillance.
Our approach to GMP
End-to-End Support
One partner from idea to registration to tender win.
Practical Guidance
Plain-language advice from people who have filed thousands of cases.
Documentation Support
Right documents, right format, right the first time.
Compliance-Focused Approach
We don't just register — we keep you compliant.
Government Procurement Expertise
We know GeM, CPP and tender portals inside-out.
Long-Term Business Support
We grow with you — from proprietorship to private limited.
Frequently asked questions
You may also need
Need Help With GMP?
Tell us about your manufacturing facility and product category, and we'll outline the applicable GMP requirements.