HACCP
HACCP
Hazard analysis and critical control points
Rs 6,000 Rs 9,000
Non IAF CertificationFinal price. No GST charged.View certificationGOOD MANUFACTURING PRACTICE
GMP Certification
Good manufacturing practice. Typically about 3 working days after complete documents, payment and review.
This certificate does not replace WHO-GMP or Schedule M certification issued by drug regulators for pharmaceutical manufacturing.
What is GMP?
Good Manufacturing Practice is a set of rules for producing goods consistently and hygienically. It covers premises, equipment, people, materials, documentation and quality control, and it aims to prevent contamination, mix-ups and errors in food, cosmetics, supplements and similar products.
Who needs it?
- Food and beverage manufacturers
- Nutraceutical and supplement makers
- Cosmetic and personal care units
- Herbal and ayurvedic product makers
Review the GMP preparation checklist
What it can do for your business
- Consistent batch quality
- Lower risk of contamination and recalls
- Meets common buyer and distributor requirements
- Prepares the unit for stricter audits
FROM APPLICATION TO DECISION
How it works
01
Define scope and buyer needs
Identify activities, sites, the standard and edition, and any buyer or tender accreditation requirement.
02
Confirm the certification route
Check the issuing body, accreditation scope, assessment arrangements and total fees in writing before payment.
03
Prepare documents and evidence
Submit initial business documents and the records needed to demonstrate how your management system operates.
04
Complete review and assessment
The applicable review or audit may require additional evidence and corrective action. Timing depends on scope and readiness.
05
Decision and ongoing review
Issuance depends on successful review, not payment alone. Check the issued scope and arrange applicable surveillance and renewal.
STARTING YOUR APPLICATION
Initial business documents
These establish who is applying and the proposed business scope. They are the starting point; the service-specific review or assessment can require additional operational evidence.
Business registration
Udyam, incorporation certificate or shop licence.
Letterhead or visiting card
Your business name and contact details.
One business invoice
A recent sales or purchase invoice.
Your business scope
What you do, in one or two clear lines.
Prepare for GMP
Use these good manufacturing practice checks to organise your preparation. For each item, identify the responsible person, the procedure used and a recent record showing what happens in practice.
- Clean, well laid out premises and controlled hygiene
- Maintained and calibrated equipment
- Control of raw materials, packaging and storage
- Written procedures and batch records
- Quality control, complaint handling and recall
Make your evidence match your scope
- Describe the actual activities and locations to be reviewed, including outsourced work and responsibilities retained by your business.
- Choose current examples from your own operation. Record the date, responsible person and outcome so the reviewer can connect the evidence to your stated scope.
- Identify missing records or unfinished actions before assessment. A policy or blank template alone does not show how a process operates.
- Ask which records apply to your selected service and scope. This preparation checklist is not an exhaustive assessment or a promise of certification.
This certificate does not replace WHO-GMP or Schedule M certification issued by drug regulators for pharmaceutical manufacturing.
BEFORE YOU COMMIT
Confirm these details in writing before payment
Use the published price alongside the agreed scope and service terms when deciding whether the offering meets your requirement.
- Scope and deliverable: the applicable standard or scheme, edition, activities, sites and exclusions, and exactly what document or support the service provides.
- Issuing or assessment body: its name and role. If accredited certification is required, confirm the accreditation body and that the relevant standard and scope are covered.
- Buyer acceptance: share the actual tender or customer clause and confirm that the proposed route meets it. A certificate title alone does not establish acceptance.
- Assessment arrangements: required documents, audit or review stages, remote or on-site work, travel, readiness requirements and expected timing.
- Fees and exclusions: the selected service price, what is included, and any separate implementation, testing, site visit, travel or statutory registration costs.
- Ongoing obligations: applicable surveillance, renewal or reassessment, their fees, and how changes to your activities or locations should be reported.
Certification and accreditation have different roles. See ISO's guidance on choosing a certification body.
ICS✓
CERTIFICATE OF REGISTRATIONNon IAF Certification
ILLUSTRATIVE LAYOUT
ILLUSTRATIVE LAYOUT
Good systems.
Great possibilities.
Great possibilities.
This is to certify that the management system of
YOUR BUSINESS NAMEhas been assessed against the requirements of
GMP
GOOD MANUFACTURING PRACTICECertificate numberSAMPLE-XXXXXNon IAF Certification
SAMPLE
Authorized
signatory
signatory
SAMPLE · NOT A VALID CERTIFICATE
A credential. Not a question mark.Independently checkable, right here.
A VERIFIABLE RECORD
More than a piece of paper.
The sample shows the layout. Issued records include your company, certified scope, applicable standard, dates and status. Specialist schemes follow their own issuer requirements.
Verify a certificateQuestions about GMP
01Is this the same as WHO-GMP?+
No. WHO-GMP and Schedule M certificates for pharmaceuticals are issued by drug regulators. This is a third-party GMP certificate.
02Who usually asks for GMP?+
Distributors, marketplaces and export buyers of food, supplements and cosmetics commonly ask for a GMP certificate.
03Can it be combined with HACCP?+
Yes. GMP provides the hygiene base and HACCP adds hazard control. See the food pack on the pricing page.
A stronger system, together.
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Rs 6,000 Rs 9,000
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