Phone: +91- 7505043946
info@nidcoherbal.com
Quality Control and Assurance
1. Fully Equipped lab with modern testing and analytical instruments
2. The Quality Assurance procedures are well documented for follow up at later stages
3. Full traceability from Raw Material to Finished Goods
4. Checking of W.I.P. to ensure standardized finished goods.
5. We have a wide range / bank of Herbs, authenticated by highly experienced Scholars and Practitioners, for proper identification of Raw Herbs.
6. The selection and grading process is done very efficiently so that no improper materials go into production.
7. Marker Compounds are identified by latest instruments like HPLC, GC, U.V. etc.
8. Microbial and Heavy Metal Testing is done on all products as per the set standards.
GMP Approved Manufacturing Facility
1. GMP Certified production facility as per the Ministry of AYUSH, Govt. of India.
2. Multiple products can be processed simultaneously at our facility as our equipment range comprises various sizes of Vertical Extractors, Soxhlet Extractor, Vacuum Drier, Tray Driers. Drum Drier and processes like vacuum distillation etc.
3. Well qualified and experienced production and analytical staff.
4. Minimum contamination ensured, while processing and material handling in all items
5. R&D for process and product development with a pilot plant.
6. E.T.P. to ensure proper waste management leaving minimum possible carbon footprints.
7. All Equipment of SS 316/304-GMP compliant and standardized grade.
8. Contactless Processing of all the herbs.
9. Lower temperature process to ensure that all the active ingredients remain unharmed.
10. Entire Extraction process is done by R.O. Water in a sanitized environment.
Storage of Raw Materials and Finished Goods
1. All materials R.M. and F.G. are stored properly in temperature controlled hygienic conditions by ensuring a moisture free environment and is even free from foreign particles.
2. The gunny bags and containers used for storage of Raw Herbs, Finished Goods and Chemicals etc are as per the GMP norms.
3. The raw matrials are stored under quarantine until samples have been drawn and tests have been performed.
4. Handling & Storage of all raw materials in the storage area are done in such a way that there is no contamination.
5. Closure and containers are capable of protecting the drug product from external conditions that may cause its contamination or deterioration.