Tüm Ekip İlaç

Hakkında

We are a specialized company on developing and manufacturing Generic Injectable Pharmaceuticals used mostly for the health of hospitalized patients.

Hikayemiz

In 2000 Tüm Ekip Pharmaceuticals is established by an Equip (team) of experts on their fields under the management of Mr. Hamza Oğuz who has 55 years of experience in Pharma sector.
We are focused on human healthcare, specialized on Hospital Pharmaceuticals. Due to our sustainable quality and accuracy in customer services, we had rapidly covered ground in the Pharma Sector.
As of today, We are the only pharmaceutical company who have 3 completely separated-dedicated sterile production area in Turkey, where we produce Injectable Carbapenems, Injectable Cephalosporins; Injectable Penicilins and Generale Formulation Injectables. We actually have over 70 product licence including all the pharmaceutical presentations.
All our designs and validation procedures are compliant with cGMP rules and conform to EMA Eudralex, Annex 1.
Tüm Ekip Pharmaceuticals is a research and development oriented generic pharmaceutical company.
The main purpose of R&D department is to develop equivalent pharmaceuticals needed in clinics and to present high quality, safe and affordable generic solutions, attaching paramount importance to quality in pharmaceuticals and to ensuring such quality with QbD principles.
To this end, the R&D department develops injectable dosage forms in compliance with the ICH guidelines.
The essence of our QA system is to be compliant with all cGXP rules.
All production, control, releases, storage, packaging and shipping activities are guaranteed by the Quality Assurance System.
Our Chemical Quality Control laboratory and Microbiological Quality Control laboratory has all the modern equipment to realize all the controls and analysis of API and finished products in house;
ISO 9001 and ISO 14001 quality certificates are also available as a part of our quality system.
All critical computerised systems are validated with the support of independent agreed consultans, to be compliant with GAMP5 (Good Automated Manufacturing Practices 5 ) and CFR 21 Part 11.