Supreme Health

Quality Regulatory

Quality Regulatory

Quality Assurance

Supreme Pharma Healthcare Pvt. Ltd. has a dedicated plant for technologically-challenging formulation across various therapeutic categories such as Analgesics (Pain Management), Gastrointestinal, Anti-Infective, Anti-Allergic, Anti-Fungal, Cardiovascular and Erectile Dysfunction. Our manufacturing facility has approval from local Drug Authority and is WHO GMP certified. We have also received accreditation from the health authorities of emerging markets.

Few of the countries are listed below:

Uganda Vietnam
Ghana Kenya
Nigeria Sri Lanka
Zambia Burkina Faso
Tanzania Cameroon
Malawi Congo

Supreme Pharma Healthcare Pvt. Ltd. has a well-established QA system to produce zero defect products. We believe in maintaining world-class business practices to ensure that our products meet all national and international standards. We follow a well-defined and thoroughly documented standard of quality procedures and systems for all our business practices.

Quality implies continuous improvement. We continuously upgrade our best practices to keep pace with the ever-changing global and regulatory requirement. Our team is driven to maintain the highest levels of quality, reliability, and transparency in order to simplify all aspects of operations. Consistency in meeting customer expectations and meeting regulatory quality and compliance norms are the true enablers and the critical differentiator that has made Supreme Health the global brand.

Our quality assurance team has developed a well-designed supply chain management system that enables us to deliver in time, enhancing our customer base by leaps over the years.

Regulatory Affairs

Supreme Health has always prioritized its product quality, which starts from the fundamental part of technical documentation necessary for regulatory dossier fillings and compliances. We have a full-fledged regulatory affairs team to provide necessary documentation support to our clients globally.

The team consists of regulatory specialists and experts who prepare dossiers in various formats (including CTD/ACTD /EUCTD etc. formats). We comply with all the regulatory requirements of different countries with their respective rules, regulations and documentation including the requirements from ministry of health for pre and post registration of the products.

To view our DMFs (Drug Master Files) filed and the Product Dossier (CTD/ACTD) list, click below

Click Here to Download DMFs Alphabetically List (A-Z)
Click Here to Download Dossier Alphabetically List (A-Z)

To view our exhaustive list of products, click here