Third Party Nutraceutical & Ayurvedic Manufacturer India | Shakumbhri Groups

WHO-GMP Certified Manufacturing
ISO 22000:2018 Standards
Advanced R&D Labs
Premium Herbal Solutions
Private Label Experts
Global Export Network
500+ Unique Formulations
WHO-GMP Certified Manufacturing
ISO 22000:2018 Standards
Advanced R&D Labs
Premium Herbal Solutions
Private Label Experts
Global Export Network
500+ Unique Formulations
Quality Control & Assurance | WHO-GMP Certified Third Party Manufacturing
Quality Control & Assurance

Quality Control for
Third Party Manufacturing

Comprehensive WHO-GMP certified quality control systems ensuring pharmaceutical excellence, regulatory compliance, and product safety for your brand’s manufacturing needs.

WHO-GMP Certified GLP Compliant GCP Standards ISO Certified FSSAI/AYUSH Approved
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Compliance Framework

International Quality Standards

Our pharmaceutical products are designed and developed in accordance with the requirements of WHO-GMP and other associated codes, ensuring global compliance and product excellence.

WHO-GMP

Production and control operations are clearly specified in written form and WHO-GMP standards are ensured throughout the manufacturing process. Our facility maintains strict adherence to Good Manufacturing Practices, guaranteeing consistent product quality, safety, and efficacy for all third-party manufacturing projects.

Good Laboratory Practice

All necessary controls on starting materials, intermediates, and finished products are ensured through rigorous GLP protocols. Our laboratory operations include comprehensive in-process controls, calibrations, validations, and analytical testing to maintain the highest quality standards in pharmaceutical manufacturing.

Good Clinical Practice

The finished product is correctly processed and checked according to defined procedures. Our GCP compliance ensures that pharmaceutical products undergo thorough quality assessment, stability testing, and batch release protocols before they reach the market, protecting patient safety and product integrity.

Quality Assurance Process

Comprehensive QC Operations

Every production batch undergoes rigorous quality control measures to ensure it meets the highest pharmaceutical standards and regulatory requirements.

01
Raw Material Qualification
All starting materials undergo strict quality testing including identity verification, purity assessment, and heavy metal/microbial contamination testing. We maintain approved vendor lists and perform thorough incoming material inspections to ensure only the highest quality ingredients enter our manufacturing process.
02
In-Process Controls
Real-time monitoring and testing throughout the manufacturing process ensures consistent product quality. Our in-process controls include physical parameter checks, chemical analysis, and microbiological testing at critical control points to identify and correct any deviations immediately.
03
Finished Product Testing
Comprehensive testing of finished products including dissolution testing, content uniformity, hardness, friability, and stability studies. Each batch undergoes complete analytical testing to ensure it meets all quality specifications and regulatory requirements before release.
04
Batch Release & Certification
Pharmaceutical products are not sold or supplied before authorized persons have certified that each production batch has been produced and controlled in accordance with marketing requirements and all relevant regulations. Our quality assurance team provides complete batch documentation and certificates of analysis.
05
Stability Studies
Ongoing stability studies under ICH guidelines ensure product quality throughout its shelf life. We conduct accelerated and long-term stability testing to determine appropriate storage conditions, shelf life, and packaging requirements for all manufactured products.
Certifications

Regulatory Compliance

Our manufacturing facility holds multiple certifications and complies with regulatory requirements of India and export destinations worldwide.

WHO-GMP
World Health Organization
ISO 9001:2015
Quality Management
AYUSH Approved
Ministry of AYUSH
FSSAI Licensed
Food Safety Standards
Why Choose Us

Benefits of Our QC System

Our comprehensive quality management system ensures your products meet the highest standards while protecting your brand reputation.

Regulatory Compliance

Manufacturing and Quality Management Operations ensure products meet customers and regulatory requirements, complying with local and international standards.

Global Export Ready

The company complies with current local regulatory requirements and the requirements of the countries where its products are exported.

Solid Dosage Expertise

Committed to the development, manufacture and supply of globally recognized solid dosage forms which are of the quality required for their intended use.

Continuous Improvement

The continuous improvement of products and manufacturing activities is an essential element of our quality policy, ensuring ongoing excellence.

Partner with Quality Excellence

Ensure your products meet the highest pharmaceutical standards with our WHO-GMP certified quality control systems. Contact us today to discuss your third-party manufacturing quality requirements.

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Common Questions

QC & Compliance FAQs

What is WHO-GMP certification?

WHO-GMP (World Health Organization Good Manufacturing Practice) is a set of guidelines ensuring pharmaceutical products are consistently produced and controlled according to quality standards. It covers all aspects of manufacturing from raw materials to finished product testing.

Do you provide batch certificates?

Yes, we provide comprehensive batch documentation including Certificate of Analysis (COA), batch manufacturing records, and stability data for every batch produced. All products are released only after thorough quality testing and approval by our quality assurance team.

What quality tests do you perform?

We perform comprehensive testing including identity tests, assay, dissolution, hardness, friability, disintegration, heavy metals, microbial limits, and stability studies. All testing follows validated methods and compendial procedures.

How do you handle regulatory audits?

We maintain complete documentation and ready-for-inspection facilities. Our quality team is experienced in handling regulatory audits from various agencies including FDA, state drug authorities, and international regulatory bodies.

Contact Us

Quality You Can Trust

Get in touch with our quality assurance team to discuss your specific requirements and learn how our QC systems can protect your brand.

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