ELEGANT CHEMICAL ENTP. PVT. LTD.
ESTD. 1998 · HYDERABAD, TELANGANA, INDIA
MULTI-PRODUCT cGMP MANUFACTURING · CMO
Every batch that leaves our facility is produced against a documented standard, verified at defined witness points, and backed by a record a principal's own auditors can review line by line.
Any authorized visitor can trace a batch from raw material to release — at any time.
These certifications sit alongside our internal quality management system, which governs manufacturing, documentation, and release across every product line at the facility. Our HALAL certification supports principal exports to the Middle East, and our Ayurvedic manufacturing license supports exports to the Middle East, South East Asia, and Russia.
Our standard operating procedures follow a single governing template, maintained and version-controlled across the facility. Sections, formats, and review cycles are standardized so that any SOP — whether for manufacturing, warehousing, or engineering — reads the same way to an auditor.
SOPs are reviewed on a defined cycle, with version history and next-review dates tracked formally rather than left to informal practice. An in-house R&D facility supports the development and market launch of new product formulations alongside this document control system.
BMR and BPR documentation for every batch produced.
IPQA checks and witness points at defined production stages.
Formal handling of out-of-specification and out-of-trend events.
PPE requirements, clean-hold validity labelling, and area clearance controls.
RO and purified water systems maintained to IP/USP norms.
AHU-controlled production areas with up to 100,000 air changes.
On-site laboratory and microbiology facility supporting release testing.
Formulation development support for new product launches.
Our QA/QC laboratory is equipped for full analytical and microbiological testing, supported by qualified, experienced technical staff. Packaging inputs are also tested in-house for strength and integrity before use.
Our documentation practices are maintained on an ongoing basis rather than assembled ahead of a scheduled audit — the intent is that any authorized visitor can trace a batch from raw material to release at any time. This discipline was recognised with an Outstanding Achievers Award from P&G for achieving 100% compliance across two consecutive quality audits.
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