Transparent, audit-ready compliance adhering to national statutory requirements, WHO-GMP guidelines, and cGMP standards at Selaqui, Dehradun.
At Ranjauly Health Care, regulatory compliance and statutory transparency form the bedrock of our manufacturing operations. Located in the pharmaceutical industrial hub of UPSIDC Selaqui, Dehradun, our facility operates under strict quality systems, validated environmental controls, and rigorous statutory registrations.
We maintain an open-door policy for institutional buyer audits and regulatory inspections. Below are our official statutory certificates and quality accreditations available for direct inspection and verification.
Review and download our verified registration credentials, statutory tax filings, and quality assurance dossiers.
Statutory certificate validating the registration of Ranjauly Health Care Private Limited under the Central Goods and Services Tax Act, covering manufacturing operations at Plot No. F-84, UPSIDC Industrial Area, Selaqui, Dehradun, Uttarakhand - 248011.
Central statutory manufacturing license granted under the Food Safety and Standards Act 2006 for dietary supplements, health supplements, nutraceuticals, protein powders, and tablets at Plot F-84, UPSIDC Selaqui, Dehradun. Valid through June 18, 2031.
Certificate of Compliance validating that manufacturing and supply of protein powder, dry syrup, protein sachet, nutraceutical tablets, hard gelatin capsules, and health supplements meet international GMP requirements. Valid through September 14, 2029.
International Quality Management System certification for high-precision manufacturing, testing, and batch distribution of nutraceutical tablets, hard gelatin capsules, protein sachets, and syrups. Valid through September 14, 2029.
Global food safety standard governing hazard analysis, critical control points (HACCP), and contamination prevention across all solid and liquid dosage manufacturing lines. Valid through September 14, 2029.
Comprehensive ISO-based Food Safety System Certification benchmarked for industrial encapsulation, cleanroom processing, and sterile packaging of healthcare and dietary products. Valid through September 14, 2029.
Our regulatory affairs team provides complete technical documentation, batch manufacturing records (BMR), and stability study dossiers for institutional and contract manufacturing partners.