/// Danışma Hattı 444 İLKO (+90 444 45 56)

Certificates and Awards

About İLKO

İLKO Pharmaceuticals pays great attention to the occupational health and safety issues and the environmental and management system in accordance with the 'High Quality Policy" in all works it conducts. Accordingly, as soon as İLKO Pharmaceuticals started its operations in 2012, it established an occupational health, occupational safety, environmental management system and obtained ISO 14001 Environmental Management System and OHSAS 18001 Occupational Health and Safety Certificates.

Furthermore, İLKO Pharmaceuticals was chosen as the "Cleanest Industrial Plant of Turkey" in 2013 by the Ministry of Environment and Urban Planning of Turkey.

In 2014, İLKO Pharmaceuticals Production Plants received confirmation of conformity to the European GMP (Good Manufacturing Practices) as a result of MHRA (Medicines and Healthcare Products Regulatory Agency of the UK) inspections.

İLKO İlaç has been registered with TS EN ISO 13485 Medical Device Production Certificate, which signifies that İLKO has the capacity and competence to produce medical devices in accordance with the principles of total quality management and GMP rules in 2017.

With this internationally validated certification, ILKO İlaç (Pharmaceutical) is able to manufacture medical devices throughout Europe, ensuring that the produced medical devices meet the legal and international requirements of the target markets.

Certificates

  • 2022
    We have the Quality Management system in accordance with the Repuclic of Turkey Ministry of Trade Authorized Economic Operator Status and approved by TSE with the TS EN ISO 9001:2015 certificate.
  • 2021
    Striving persistently to build the future today, Ilko Pharmaceuticals has added a new item to its care for the environment. The Zero Waste Management Program, which is effectively conducted at Ilko’s Production Facilities, has fulfilled all related requirements of the Zero Waste Directive that was published and enforced on the Official Gazette dated 12 June 2019 and no. 30829, and it has been certified by the Ministry of Environment and Urban Planning of the Republic of Turkey.
  • 2021
    İLKO Pharmaceuticals has obtained OHSAS 18001 certification upon initiation of company operations which was originally developed by British Standards Institute and currently the standard is replaced with international occupational health and safety standard ISO 45001. İLKO Pharmaceuticals has successfully completed this transition by obtaining the ISO 45001 certification. Built on OHSAS 18001 standard, ISO 45001 Occupational Health and Safety Management System has a high-level structure established for ISO management system standards and allows for risk-based management of processes by integration into existing quality systems.
  • 2019
    ILKO Pharmaceuticals has been entitled to receive both BS 10012 Data Protection Personal Information Management System and ISO 27001 Information Security Management System certificates that determine the confidentiality, integrity and accessibility of personal information at international standards. The latter institution has these documents in Turkey, was the first and only company in the pharmaceutical sector ILKO Pharmaceuticals.
  • 2019
    ILKO Pharmaceuticals has obtained Malta European GMP certificate.
  • 2017
    ILKO Pharmaceuticals has been certified with TS EN ISO 13485, the Medical Device Production Certificate, in which it has the capacity and competence to manufacture medical devices in accordance with the principles of total quality management and GMP rules. With this internationally validated certification, ILKO Pharmaceuticals is not only a manufacturer of medical devices throughout Europe, but also fully meets the legal and international requirements of the medical devices in the target markets.
  • 2014
    ILKO Pharmaceuticals Production Facilities received the certificate of conformity to European GMP (Good Manufacturing Practices) following the audits carried out by MHRA, the Ministry of Health, Pharmaceutical Supervision Agency of the UK.
  • 2012
    As soon as ILKO Pharmaceuticals started its operations, it established ISO 14001 Environmental Management System and OHSAS 18001 Occupational Health and Safety certificates by establishing occupational health, safety and environmental management system.

Awards

  • 2016
    Golden Mortar Awards 2016 R&D award was given to ILKO with morphine sulfate tablet.
  • 2016
    ILKO Pharmaceuticals, Turkey's first indigenous morphine sulfate tablets with TUBITAK, TTGV and large firms jointly carried out jointly by TUSIAD 2016 Technology Awards Contest - Grand Prize was the owner of the product category.
  • 2013
    ILKO Pharmaceuticals was chosen Turkey’s Clean Industry Plant by the Republic of Turkey Ministry of Environment and Health in 2013.
  • 2012
    ILKO Pharmaceuticals has been awarded with the Environmental Certificate as a result of its studies on environmental protection, development, prevention of pollution and dissemination of environmental certificate.
TURKISH

Özgeçmiş Ekle

Acknowledgement ​and Consent Letter regarding the processing and preservation of my CV.

ACKNOWLEDGEMENT AND CONSENT LETTER

ACKNOWLEDGEMENT AND CONSENT LETTER

This Acknowledgement and Consent Letter has been prepared by SELÇUKLU HOLDİNG A.Ş. and the group companies directly or indirectly controlled by SELÇUKLU HOLDİNG A.Ş. (“Company”) in accordance with Personal Data Protection Law No. 6698 (“Law”) on the purpose of clarifying data owners during the official web sites visits process regarding the procedures and principles on processing of personal data and special categories of personal data provided by data owners as well as receiving their consent about processing data within the scope and by purposes stated below.

The following terms used in this Acknowledgement and Consent Letter shall have the below stated meanings;

"personal data”; any information relating to an identified or identifiable natural person (Visitor),

“processing of personal data”; any operation which is performed on personal data such as collection, recording, storage, preservation, alteration, adaptation, disclosure, transfer, taking over, making available for collection, categorization or blocking its use by wholly or partly automatic means or otherwise than by automatic means which form part of a filing system,

“special categories of personal data”; race, ethnic origin, political opinion, philosophical belief, religion, sect or other beliefs, appearance and dressing, membership of association, foundation or trade-union, health, sexual life, criminal conviction and data regarding the safety measures, biometric and genetic data of the person (Visitor),

a) Regarding the Data Controller
Your personal data and your data evaluated as special categories of your personal data which you have shared with us such as e-catalog template, e-bulletin registration, contact form filling, product quality / complaint notification, medical information request, side effect / adverse reaction notification can be processed by the Company as per the Law within the scope and by purposes stated below. Pursuant to the Law, the Company is accepted as the data controller.
b) Purposes of Processing Your Personal Data
Your personal data and your data evaluated as special categories of your personal data which you have shared with us such as e-catalog template, e-bulletin registration, contact form filling, product quality / complaint notification, medical information request, side effect / adverse reaction notification are processed in compliance with the conditions stipulated under Article 5 and 6 of the Law regarding the processing of personal data. Purposes of processing your personal data and your data evaluated as special categories of your personal data which you have shared with us such as e-catalog template, e-bulletin registration, contact form filling, product quality / complaint notification, medical information request, side effect / adverse reaction notification includes without any limitation: The Company’s legal obligations and service policies.
c) Transference of Your Personal Data
Your personal data and your data evaluated as special categories of your personal data which you have shared with us such as e-catalog template, e-bulletin registration, contact form filling, product quality / complaint notification, medical information request, side effect / adverse reaction notification can be transferred to the Company’s group companies, subsidiaries, shareholders, partners with limited to the fulfillment of the purposes mentioned in the item b) in compliance with the conditions stipulated under Article 8 and 9 of the Law and your data can be processed by those institutions.
d) Method and Legal Reason of Personal Data Collection
Your personal data and your data evaluated as special categories of your personal data which you have shared


with us such as e-catalog template, e-bulletin registration, contact form filling, product quality / complaint notification,


medical information request, side effect / adverse reaction notification are collected upon filling up this form as a data owner and/or through the information and documents that you submit during your visit. Your personal data and your data evaluated as special categories of your personal data which you have shared with us such as e-catalog template, e-bulletin registration, contact form filling, product quality / complaint notification, medical information request, side effect / adverse reaction notification collected with legal reasons mentioned above can be processed and transferred being subject to the item b) and item c) of this Acknowledgement and Consent Letter within the scope of processing conditions and purposes stated under Article 5 and 6 of the Law.

e) Rights of Personal Data Owner Stated under Article 11 of the Law
In accordance with Article 11 of the Law, data owners have a right to
• Learn whether the personal data is processed,
• Request information regarding personal data processing,
• Learn the purpose of processing the personal data and whether such data are used pursuant to their purpose,
• Know the third persons in the country and abroad to whom the personal data has been transferred,
• Request rectification in case the personal data has been processed incompletely or inaccurately and request the third parties whom the personal data has been transferred to be notified in terms of this processing,
• Demand the deletion or destruction of the personal data in the event that the reasons for its processing cease to exist despite the fact that it has been processed in accordance with the provisions of the Law and the other related provisions of law and request the third parties whom the personal data has been transferred to be notified in terms of this processing,
• Object to any result that is against him/her as a result of the exclusive analysis of the processed personal data via automatic systems,
• Request the recovery of the loss in case he/she suffers damage due to unlawful processing of the personal data.

I agree, declare and undertake that I, as the data owner, have been informed precisely as per the Article 11 of the Law, with respect to my rights as a data owner and for the duration of 5 (five) years beginning from the signing date of this Acknowledgement and Consent Letter, my personal data and data evaluated as special categories of my personal data which I have shared with your party during my visit can be kept, processed, used, transferred by the Company or/and the data processor assigned by the Company, also be processed by the people/institutions to whom the data has been transferred.

Visitor
Name/Surname:
Date:
Signature:

 

Group Companies of Selçuklu Holding A.Ş.;

İlko İlaç San. Ve Tic. A.Ş.
İlkogen İlaç San. Ve Tic. A.Ş.
Selin İnş. Ve Tic. A.Ş.
Penta Perakende Mağazacılık A.Ş.
Costa Sağlık Spor Hizm. Tic. Ltd. Şti.
Almesan Alüminyum San. Ve Tic. A.Ş.
Mehtap Mutfak Eşyaları San. Ve Tic. A.Ş.
Sentez Grup Ambalaj San. Ve Tic. A.Ş.