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Laafon Galaxy Pharmaceuticals
  • Products, Injectables

Diclofenac Injection 75mg/ml: MOA, IM/IV Dose (mL) & Limits

laadic injection

At a glance · for healthcare professionals Diclofenac sodium injection 75 mg/mL: action, dose and limits How it works: it blocks both COX-1 and COX-2, so less arachidonic acid is converted into the prostaglandins that drive pain, inflammation and fever.[1]…

  • Darshan Singh
  • October 8, 2026
  • SOP

SOP for Preparation of Sanitizing Solution in Pharma: 7 Dilutions

Sanitizing solution in pharma preparation flow: check stock CoA, calculate V1 = C2 x V2 / C1, dilute, sterile-filter for Grade A and B, label and record, use within the in-use period

Short answer A sanitizing solution is a disinfectant concentrate diluted to a fixed, validated in-use strength. A common error in published SOPs is writing the dilution as a volume of stock without stating the stock’s strength. Forty millilitres of hydrogen…

  • Darshan Singh
  • October 5, 2026
  • Pharma Company, Drugact, Third-party-mfg

Agreement for Marketing Format: Free 2026 Download

Agreement for marketing format for pharma companies under Rule 84D

Regulatory guide · Drugs and Cosmetics Rules, 1945 Written by Darshan Singh, M.Sc. (Organic Chemistry), 23+ years in pharmaceutical QA, QC and drug regulatory affairs · Published 15 February 2023 · Updated 4 October 2026 On this pageWhich routeWhat changedSample…

  • Darshan Singh
  • October 4, 2026
  • SOP

SOP for Pest Control in Pharmaceutical Industry: Rodents, Insects & Birds

Pest control in pharmaceutical industry: 5-zone device plan showing exterior bait stations, internal non-toxic monitors, insect light traps, air curtains and bird netting

By Darshan Singh, QA/QC and regulatory practitioner (23+ years). Rebuilt 3 October 2026 against the notified Revised Schedule M text. Short answer Pest control in a pharmaceutical plant is a written GMP obligation. Revised Schedule M requires premises that keep…

  • Darshan Singh
  • October 3, 2026
  • Pharma Company

Alu Alu Packing: 6 Stations, Leak Tests & Costly Mistakes

Alu Alu packing cold-form blister of tablets

Packaging machinery guide By Darshan Singh, 23+ years in pharma QA, QC and regulatory affairs Updated 2 Oct 2026 Short answer Alu Alu packing is a cold-form blister. A three-layer oPA/aluminium/PVC laminate is pressed cold into pockets, the tablets drop…

  • Darshan Singh
  • October 3, 2026
  • Pharma Company

Tablet Compression Machine: 5 Essential Stages, CPPs & Fixes

Tablet compression machine working principle: rotary tablet press

Working principle in one paragraph A tablet compression machine (tablet press) makes a tablet by squeezing a measured volume of powder or granules between an upper and a lower punch inside a die. On a rotary press the turret carries…

  • Darshan Singh
  • October 1, 2026
  • Pharma Company

Quality Control in Pharmaceutical Industry: 6 Proven Rules

Quality control in pharmaceutical industry: analyst in blue gloves transferring a blue solution from a flask to a test tube

Quality control in pharmaceutical industry · Revised Schedule M, Part I, section 19 Reviewed by Darshan Singh · first published 25 Feb 2023 · rebuilt and fact-checked 1 Oct 2026 Quality control in pharmaceutical industry: what QC does Quality control…

  • Darshan Singh
  • October 1, 2026
  • SOP

Validation in Pharmaceutical Industry: Schedule M, VMP & 3-Batch Rule

Validation in pharmaceutical industry lifecycle diagram: URS, DQ, FAT/SAT, IQ, OQ, PQ, process validation and ongoing verification mapped to EU GMP Annex 15 clauses, FDA 2011 stages and Schedule M clause 5.3

By Darshan Singh, 23 years in pharmaceutical QC, QA and regulatory affairs · Reviewed against the source texts on 29 September 2026 Short answer Validation is documented evidence that premises, utilities, equipment, processes, cleaning procedures, test methods and computerised systems…

  • Darshan Singh
  • September 30, 2026
  • SOP

Batch Record Review in Pharmaceutical Industry: SOP + 20 Checks

Batch record review in pharmaceutical industry flow: executed batch processing and packaging records pass production review, QC record review, QA review and authorised person certification before release, with the discrepancy investigation path to CAPA and the product quality review

By Darshan Singh, 23 years in pharmaceutical QC, QA and regulatory affairs. Clauses checked against the primary texts on 27 Sep 2026. Short answer Batch record review is the check, made for every batch before it is released, that the…

  • Darshan Singh
  • September 27, 2026
  • SOP

SOP for Conductivity Meter Calibration: USP 645 Limits, KCl Table

Conductivity meter calibration diagram: two-electrode cell with cell constant K = L/A, temperature sensor, cable and meter in a KCl standard

Short answer A conductivity meter is calibrated in two independent parts. First, the cell constant is established with a standard solution of known conductivity. Second, the meter electronics are checked against traceable precision resistors. For pharmacopoeial water testing, USP <645>…

  • Darshan Singh
  • September 27, 2026
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