Our Expertise

 With decades of experience in the pharmaceutical industry, we have developed a deep understanding of the complexities involved in producing generic medications. Our team of experts combines scientific knowledge, technological innovation, and regulatory compliance to develop and manufacture pharmaceutical products that meet the highest quality standards. We continually invest in research and development to expand our product portfolio, ensuring that we address the evolving healthcare needs of patients worldwide. 

 We specialize in overseeing critical aspects including pharmacovigilance, chargebacks, FDA product registrations, and Medicaid/Medicare submissions. Covalence excels at negotiating contracts across various trade sectors and offers unparalleled distribution capabilities compared to other companies.  

 With a proven track record of exceptional performance in delivery, customer service, sales, and supply chain management, as well as strong relationships with major customers, Covalence stands as an outstanding ally for your commercialization requirements.

Covalence possesses the capability to collaborate effectively with both multinational and regional partners, enabling the joint development of products and their successful introduction to the market. We take pride in being the preferred partner for product development, contract formulation development, and technology transfers.

Covalence actively seeks partnership opportunities to license 505(B)(2) NDAs, FDA-approved ANDAs and authorized generics. Furthermore, we are keen on forging co-marketing alliances for products that are still in the developmental stage.

Our current portfolio is the result of internal research and development efforts. Supported by a dedicated sales and marketing team, our US division is fully prepared to introduce collaborative projects to the American marketplace.

If you are a potential partner seeking collaboration in the aforementioned areas, we encourage you to get in touch with us today.