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Global presence

Global Presence

Currently, Qualence Life Sciences exports to 26 countries and five continents in the world, including Africa, South-East Asia, North America, CIS, and Latin America. With over a number of international product registrations (still expanding), we are emerging as a major potential Indian pharmaceutical manufacturer.

In an effort to streamline the export vision at Qualence Life Sciences, a dedicated Export Regulation department has been created to handle international audits and to provide complete export documentation, including COAs, COPPs, and COOs, as well as dossier preparations in the CTD format. Qualence Life Sciences manufacturing facility operates completely in compliance with cGMP standards and has been certified by numerous regulatory agencies.

By providing superior performance and high-quality products at the right price, we strive to be the premier pharmaceutical manufacturer for India and neighboring countries. The formulation development team and regulatory department of our company are dedicated to bringing the latest generics to our markets, ensuring that our customers are always receiving the latest products.

Asia

Myanmar, Philippines, Bahrain, Dubai, Hong kong, Singapore, Thailand, Israel, Jordan, Sri Lanka, Cambodia, Russia, Saudi Arabia, Singapore, Syria, Turkey, Turkmenistan, Uzbekistan, Yemen, Vietnam, Indonesia, Malaysia, Iran, Iraq, Tajikistan.

Africa

South Africa, Sudan, Tunisia, Ghana, Nigeria, Kenya, DRC, Namibia, Somalia, Guinea, Togo, Burkina Faso, Mali, DRC, Egypt, Ethiopia, South Sudan, Niger, Chad.

North & Latin America

USA, Canada, Panama, Trinidad and Tobago, Costa Rica, Puerto Rico, Dominican Republic, Argentina, Guatemala, Guyana, Peru, Bolivia, Venezuela, Brazil, Bahamas, Ecuador

Europe

Austria, Azerbaijan, Belarus, Belgium, Cyprus, Czech Republic, Denmark, France, Georgia, Germany, Hungary, Ireland, Iceland, Netherlands, Norway, Poland, Spain, Sweden, Switzerland, Ukraine, United Kingdom (UK), Latvia

Oceania

Australia, New Zealand, Fiji.

Policy on Partnering

We believe in working together toward success with mutual understanding, trust, and understanding of what our partners expect from us, as well as satisfying their needs.

Collaborations

We assist our clients by providing the best price, accurate artwork, and full support for regulatory documents, promotional materials, and other sudden requirements, as well as marketing support, which is also provided by our team.

Labeling of private products

Private Labeling is a highly customized service that is provided according to the client’s specifications. We strive to develop products that are specific to the requirements of our customers located in various parts of the world in order to satisfy their diverse needs.

The Regulatory Services Division 

This team consists of an elite, highly qualified group of professionals who provide necessary information for ensuring our products are of the highest quality, safety, and efficacy. In most countries, our products require clinical trials, FDA certificates, and BE studies for registration according to the guidelines of the respective ministries of health.

Delivery & Dispatch

Our company understands that pharmaceutical products must be distributed with the utmost care and attention. Finished products and raw materials awaiting processing are stored in modern, fully climate-controlled high-bay storage areas. By utilizing its modern data and order processing systems, its inspections of all goods entering and leaving the factory, and the most advanced transportation logistics (road, sea, and air), we are able to meet the delivery needs of our customers. It does not matter how long it takes for the product to reach its destination, or the route it takes. It is carefully monitored throughout its journey.

Essentially, the following factors have contributed to our success in manufacturing drugs for overseas markets:

  • Highest quality products.
  • 24 hour customer service.
  • On-time delivery.
  • Quality products at competitive prices.
  • High compliance rate.
  • Facilities that are WHO-GMP certified.
  • An FDA-approved facility.
  • Complete regulatory support.