GMP Compliant Plant J.K. Road Industrial Area, Govindpura, Bhopal, Madhya Pradesh
State-of-the-Art Pharmaceutical Plant

Manufacturing Infrastructure & QC Testing

A deep look inside Adhish Industries' licensed manufacturing plant in Bhopal, featuring humidity-controlled cleanrooms, high-output rotary tableting, and rigorous HPLC analytical quality assurance.

01

Rotary Tableting Compression

Equipped with multi-station high-speed rotary tablet presses designed for precise weight variation and hardness control. Capable of manufacturing effervescent tablets ranging from micro 4mg doses up to heavy industrial 3.5g blocks.

  • ✓ Output: 500,000+ tablets per single shift
  • ✓ Tight weight uniformity within ±2% margin
  • ✓ Controlled compression force to ensure rapid dissolution
02

Dehumidified Cleanrooms

Sodium Dichloroisocyanurate (NaDCC) and effervescent binders are sensitive to moisture. Our compression and packaging bays are isolated inside Class 100,000 cleanrooms maintained below 35% relative humidity (RH).

  • ✓ Industrial desiccant dehumidifiers running 24/7
  • ✓ HEPA-filtered air circulation prevents contamination
  • ✓ Guarantees 3-year commercial shelf stability
03

Analytical In-House Laboratory

Every raw material and finished tablet batch is chemically verified by our QA chemists. Testing protocols adhere strictly to Indian Pharmacopoeia (IP), British Pharmacopoeia (BP), and WHO water treatment monographs.

  • ✓ Available Chlorine (FAC) iodometric titration
  • ✓ Disintegration timer (Effervescence < 3 mins)
  • ✓ Digital Karl Fischer moisture titrators
GMP Process Flow

From Raw Compound to Sealed Bottle

Our certified 6-step manufacturing protocol ensures complete traceability for each commercial batch.

STEP 01

Raw Material Assay Verification

Raw NaDCC and stabilizers are tested for active chlorine percentage, moisture content, and heavy metal limits prior to release into production.

STEP 02

Precision Blending & Granulation

Active compounds are blended with pharmaceutical effervescent agents (food-grade bicarbonates and organic acid carriers) in double-cone blenders.

STEP 03

Controlled Cleanroom Compression

Tablets are stamped on rotary presses with continuous weight monitoring, thickness checks, and friability testing at 30-minute intervals.

STEP 04

Hermetic Induction Packaging

Immediate packaging into moisture-barrier HDPE bottles or Alu-Alu tropicalized blister foil to lock out ambient humidity.

STEP 05

Quarantine & Microbiological Release

Finished batches enter climate-controlled quarantine while 72-hour dissolution and titration assays are recorded in the batch log.

STEP 06

COA Issue & Logistics Dispatch

Each master carton is coded with batch numbers, manufacturing/expiry dates, and dispatched with an official Certificate of Analysis (COA).

Schedule an On-Site Facility Audit

We welcome quality auditors from government health bodies, NGOs, and export trading houses to inspect our Bhopal plant.