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7 YEARS SECTOR EXPERIENCE

TECRÜBE 90%

OUR GOAL IS TO PROVIDE YOU HIGH QUALITY & ECONOMICAL SOLUTIONS

DeltaPV was established in 2011. Our company conducts pharmacovigilance activities for over 180 companies in accordance with the related regulations and guidelines, with its expert team of pharmacists. DeltaPV is working with a broad range of pharmaceutical companies consisting of licensor firms, local companies, global firms and their local affiliates.

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PHARMACOVIGILANCE SERVICES

According to the ” Regulation On The Safety Of Medicines” published in the Official Gazette on April 15, 2014, the pharmacovigilance obligations of the pharmaceutical companies which have a license or are on the license application have increased. DeltaPV undertakes all pharmacovigilance operations of the pharmaceutical companies in accordance with the Guidance on Good Pharmacovigilance Practices.

WE CONTINUE TO WORK FOR BETTER.
DELTAPV IN NUMBERS

58 +

Number of countries we work in.

180 +

Number of Audits and inspections

82 +

Number of Companies we are working with

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Reporting of suspected adverse reactions and side effects.

After a medicinal product is licensed, reporting of suspected adverse reactions has great importance. If any side effect which is present or absent in the patient information leaflet occurs, please contact your doctor, pharmacist or nurse. Reporting of the adverse reactions allows the continuous monitoring of the medicinal product’s benefit/risk ratio. Health professionals are obliged to report any suspected adverse reactions to Turkish Pharmacovigilance Centre (TUFAM). (www.titck.gov.tr; e- mail: tufam@titck.gov.tr; tel: 0 800 314 00 08; fax: 0 312 218 35 99).

Notify any side effects to Turkish Pharmacovigilance Centre (TUFAM) by clicking the “İlaç Yan Etki Bildirimi” icon on www.titck.gov.tr; website, by sending an email to tufam@titck.gov.tr or by calling 0 800 314 00 08 side effect reporting line. Reporting any side effects experienced allows more information to be gathered about the drug in use.