Quality You Can Verify. Standards You Can Trust.
Our Commitment to Quality Is Documented
At Makin Laboratories, quality is not a claim; it is a system. Every certification we hold has been independently assessed and issued by a recognised authority. Every batch we manufacture undergoes rigorous testing against pre-approved specifications before it leaves our facility. This process ensures that all products meet our quality standards prior to distribution.
This page is your reference for Makin's compliance credentials, quality control processes, and in-house testing capabilities.
Our Certifications
All certifications are independently assessed and issued by recognised authorities.
01 International quality standards
02 GMP certifications
03 Country regulatory approvals
04 Market-specific certifications
Three-Stage Quality Control For Every Batch
No material or product proceeds to the next stage or leaves our facility without successfully passing each stage of our quality testing process.
Raw Material Testing
- Identity verification
- Potency and standardisation confirmation
- Heavy metals screening
- Pesticide residue testing
- Microbial contamination testing
- Aflatoxin and mycotoxin screening
In-Process Testing
- Blend uniformity
- Weight variation
- Hardness and friability of tablets
- Fill weight capsules and softgels
- Disintegration testing
- Process monitoring at each stage
Finished Product Testing
- Active ingredient assay
- Microbial limits as per the applicable pharmacopoeia
- Heavy metals: Lead, Arsenic, Cadmium, Mercury
- Stability-indicating methods
- Certificate of Analysis issued for every batch
In-House Quality Control Laboratory
Our in-house QC laboratory supports formulation development, raw material qualification, and batch release testing. Core analytical and physical testing is conducted on-site, enabling faster turnaround and direct quality oversight at every stage of manufacturing.
Heavy metal testing is conducted by accredited external laboratories as required, ensuring the highest analytical standards for safety-critical parameters.
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High Performance Liquid Chromatography HPLC
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Gas Chromatography GC
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UV-Vis Spectrophotometer UV-Vis
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Karl Fischer Titrator moisture analysis
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Atomic Absorption Spectrophotometer AAS
Documentation With Every Batch
Batch Manufacturing Record
Complete production documentation for every batch manufactured.
Raw Material Test Reports
Supplier qualification, incoming material test documentation and raw material test reports.
Certificate of Analysis
Complete production documentation, including batch record for every batch manufactured.
Export Documentation
Certificate of Origin, Health Certificate, Free Sale Certificate on request, as required for your market.
Our Manufacturing Facility
Manufacturing since 2013 at the Pithampur facility
Facility established on 5.5 acres of land in Sector III, Industrial Area, Pithampur
First WHO-GMP Certified Facility in Central India (Certified in 2018)
Manufacturing Site
Plot No. 36-B, 48, Sector III, Pithampur, Dist. Dhar, Madhya Pradesh, 454774 India
Registered Office
33, Narmada Nagar, Annapurna Road, Indore, Madhya Pradesh, 452009 India
Discuss Your Requirements
Tell us your target market and regulatory requirements. We will confirm which certifications apply to your specific needs.
Contact Our Team →Request Certificate Copies
GMP certificates, CoA samples, and compliance documentation available for qualified buyers.
Request Certificates →