Trulip Pharma

Maintaining the highest standards :

• At Trulip Pharma, we accept nothing but the highest attainable quality and safety standards and demand the same high standards of our suppliers and distributors.
• Our standards are maintained through strict policies and procedures. These procedures are carefully implemented and are applicable throughout the lifecycle of the product, from development to commercialization.
• The company is assessed regularly by the Agency to ensure that Trulip Pharma is certified to be registered in the list of Registered Organizations with regard to the Standard and scope of supply. GMP is the regulatory regime all pharmaceuticals manufacturers must comply with to ensure that the finished products possess the requisite identity, strength, quality, and purity and to ensure the safety of the patients.

High Quality Production :

• All manufacturers with whom Trulip Pharmaceuticals cooperates are carefully inspected by Trulip Pharma quality assurance division at regular intervals to ensure compliance for pharmaceuticals manufacturing. The company's manufacturers must be licensed by the Indian Medicines Agency and are inspected by that agency regularly.
• Finally, the company's QP releases the pharmaceutical product for sale. The release is conditional on all analysis results meeting specifications and on the pharmaceutical having been manufactured, packaged and tested in accordance with GMP requirements and the approved marketing authorization.

Safety Monitoring :

• Trulip Pharma Pharmacovigilance team is responsible for monitoring, identifying, analyzing and reporting potential safety risks. The team actively reviews patient safety experiences, and uses an advanced database that allows for effective collection, assessment and prevention of adverse events.
• We are continuously monitored by regulatory authorities. As a marketing licence holder the company must meet the requirement of monitoring the safety of the products approved for use on the world market.

Pharmaceuticals and the Environment :

• Trulip Pharma complies with all environmental legislation and requirements currently governing pharmaceuticals manufacturing. Consequently, the company verifies that manufacturers hold environmental permits and ensures that the results of analyses from test samples meet the requirements stipulated in environmental permits. In addition, Trulip Pharmaceuticals verifies that the manufacturers analyse the water which leaves their plants for traces of pharmaceutical substances and Trulip Pharmaceuticals scrutinises the way in which manufacturers handle their waste.
• Trulip Pharmaceuticals ambition is to constantly improve its work on environmental issues and Trulip Pharmaceuticals carefully monitors the areas on the agenda of public agencies.