WELCOME TO SCOTMANN

Scotmann is a pharmaceutical centre of excellence with a diversified portfolio of branded generics in biotech, cardiovascular, diabetes, gastroenterology, respiratory, inflammatory diseases, pain management, osteoporosis, psychiatry and OTC segments.

Our R&D is structured around partnerships with European Contract Research Organizations (CROs). These partnerships help us adhere to excellent manufacturing practices, ensuring that our products meet highest International standards for safety and efficacy.

Living up to your high expectations

Meeting complex specifications with a consistently productive packaging process

Scotmann’s manufacturing processes are contained within complete HEPA/ULPA ceiling Class 100 “Clean Rooms” supported by a series of class 10000 ...

Active pharmaceutical ingredients

Scotmann directly procures only the highest-grade APIs having not less than 90% shelf life from proven and reputable sources. All ...

Formulations

Scotmann’s formulations are developed by highly skilled and experienced team of professionals, The formulations are subjected to internationally accepted stability ...

Quality control

Each product at Scotmann undergoes strict quality control checks and testing procedures before reaching the consumer. At each stage of ...

Quarantine & inspection procedures

In order to ensure that every material received is pure and unadulterated, it is quarantined after being received at the ...

Processing

Once an ingredient is approved by (QA) for processing, the product goes through multiple control points throughout the production process. ...

Sanitation

Sanitation is a vital component of producing high quality products, which is why Scotmann conducts periodic as well as random ...

Testing

Scotmann uses state-of-the-art analytical equipment for testing raw materials, inprocess materials and finished products. Our laboratories use scientifically validated testing ...

State of the art water purification system

Scotmann’s water purification system combines double Reverse Osmosis (RO) and ultra pure water technology for the production of high quality ...

Identification

Scotmann uses state of the art, FDA 21 CFR (Code of Federal Regulations Part 11) compliant Shimadzu Prominence i -LC-20AT HPLC and Shimadzu Fourier Transform Infra-Red Spectrophotometer (FTIR) equipped with Attenuated Total Reflectance (ATR) technology to identify and characterize the chemical entity of APIs and finished products.

Purity, Potency & Organic Impurities

Scotmann assures the purity and potency of APIs and finished products by using FDA 21 CFR (Code of Federal Regulations Part 11) compliant Shimadzu Prominence i -LC-20AT HPLCs.

Elemental Impurities & Heavy Metals

Screening of APIs for any toxicity or carcinogenicity related to residual solvents is analyzed on FDA 21 CFR (Code of Federal Regulations Part 11) compliant Shimadzu GC-MS (Gas Chromatography - Mass Spectrometry) & Agilent GC (Gas Chromatography).

Residual Solvents

Screening of APIs for any toxicity or carcinogenicity related to residual solvents is analyzed on FDA 21 CFR (Code of Federal Regulations Part 11) compliant Shimadzu GC-MS (Gas Chromatography - Mass Spectrometry) & Agilent GC (Gas Chromatography).

Bioequivalence In-Vitro Studies

In-vitro product dissolution profile / bioequivalence of finished products is determined by extensive dissolution studies.

SGS Certification

SGS S. A. Geneva, Switzerland certified Quality Management System (QMS) for inspection, verification & testing.

TUV Halal Certification

Halal Food Quality Management System is certified by TUV Austria Bureau of Inspection & Certification.

PNAC Certification

Scotmann's Quality Control Lab is ISO/IEC 17025 accredited for regular surveillance and compliance with the requirements of PNAC (Pakistan National Accreditation Council) as per Accreditation Certificate Number: LAB-188.