Product Certifications

GMP Certification

GMP WHO-GMP Pharmaceutical Cleanroom Assembly Line
Standard Compliance Support

GMP is the baseline requirement for any pharma manufacturer, cosmetics maker, or supplement producer. If you want WHO-GMP certification (required for most drug export markets), or if your State Licensing Authority audit requires it, GMP is where you start. We've done GMP setups for pharmaceutical units in Baddi, Haridwar, and Hyderabad, we know what drug inspectors look for in your facility, not just what the textbook says.

We Take Care of Everything

From preparing your documents to training your team and supporting you during the final audit, we handle the entire process. You focus on running your business, we make sure you get certified.

What You Gain From This Certification

Here is how this certification helps your business grow and win more clients:

Proves your factory follows proper hygiene and quality standards

Reduces contamination, mix-ups, and production defects

Builds buyer and consumer trust in your manufactured products

How Long Does It Take

Standard completion schedule vs priority fast-track certificate issuance options:

Standard Timeline

5 to 10 Working Days

⚡ NEED IT FASTER?

Express Priority Issuance

Need it faster for an urgent tender deadline or buyer audit? We expedite audit slot allocation & filing.

Same-Day Filing & Fast Audit
Express Registrar Allocation
Urgent Tender & Audit Guarantee

Documents You Will Need

ISO & compliance certifications require minimal business proof (GST or PAN). Don't worry if any paperwork is missing — our experts assist with drafting and preparing everything for you.

100% Paperwork Support: We handle technical drafting, formatting, and file preparation.

Product Technical Data Sheet & Drawings

Existing Product Test Reports (if any)

Raw Materials Certificate of Analysis (COA) / Specifications

Manufacturing Process Flowchart & Plant Layout Map

Product User Guides or Safety Instruction Leaflets

How We Get You Certified: Step-by-Step

Here is exactly what happens from the day you contact us to the day you get your certificate:

01

Standard Identification

We evaluate your product's design and features to determine the exact compliance directives and standards needed.

02

Sample Testing & Coordination

We coordinate sample submission to accredited labs and track testing reports to ensure your product meets target limits.

03

Technical File Preparation

We compile all lab test reports, user manuals, declarations of conformity, and drawings into a complete Technical File.

04

Factory Production Audit

We check and optimize your factory production line controls to satisfy standard requirements.

05

Marking & Certification

Receive the official test certifications and approval to apply compliance labels (like CE/RoHS) to your products.

Who Needs This?

This certification is commonly needed by businesses in these industries:

Pharmaceutical & Drug Manufacturers

Nutraceuticals & Supplement Brands

Cosmetics & Skincare Formulation

Ayurvedic & Herbal Labs

Ayurvedic & Herbal Medicine Units

Cosmetics & Toiletries Factories

Nutraceutical Capsules & Tablets

API & Chemical Drug Units

Why Businesses Choose Us

Here is what you can expect when you work with us:

Dedicated Audit Support

We stand with you through every step until your certificate, license, or audit report is fully approved.

Experienced Lead Auditors

Our consultants are seasoned audit specialists with over 6 years of hands-on certification experience.

No Hidden Costs

We quote flat, all-inclusive fees covering setup, consultation, coordination, and final approvals.

End-to-End Handholding

We do not just tell you what to do; we write the documents, train your staff, and handle the inspectors.

Lifetime Advisory Support

Get continuous assistance for annual surveillance audits, compliance renewals, and standard updates.

Common Questions

Answers to the questions we hear most often about this certification:

Pharmaceutical companies need it for their drug manufacturing license and WHO-GMP for exports. Cosmetics and supplement makers need it for quality assurance. If your State Drug Inspector is coming for a license audit, GMP compliance is exactly what they check.

For most international certifications like CE and RoHS, yes: your product needs to be tested at an approved lab. We arrange the testing and handle all the paperwork for you.

Yes, if you change your product design or materials without informing the certification body, your certificate can be suspended. We help you manage any product changes properly so this does not happen.