TAK Pharma sp. z o.o. is a pharmaceutical regulatory affairs consulting company established in 2004, based in Warsaw, Poland.

Ensuring compliance with government regulations and guidelines to facilitate the approval, registration, and ongoing compliance of pharmaceutical products.

Monitoring the safety profile of drugs to identify, evaluate, and prevent adverse effects, contributing to the overall safety of pharmaceutical products.

Strategically determining the optimal pricing for pharmaceutical products and navigating reimbursement processes to maximize market access and affordability.

Assessing the clarity and comprehensibility of written materials related to pharmaceutical products, ensuring that information is easily understood by diverse audiences.

Providing accurate and culturally appropriate translations of medical documents between Polish, English, and French to facilitate global communication in the healthcare industry.

Evaluating and ensuring compliance of promotional materials with regulatory standards, safeguarding the accuracy and appropriateness of marketing content for pharmaceutical products.

Managing the regulatory processes for medical devices, including obtaining necessary approvals, ensuring conformity with quality standards, and addressing safety concerns to meet regulatory requirements imposed by health authorities.

Navigating regulatory frameworks to ensure compliance with safety standards, labeling requirements, and permissible ingredients for food supplements, and securing necessary approvals for marketing and distribution.

Adhering to regulatory guidelines to ensure the safety, quality, and labeling accuracy of cosmetic products, obtaining necessary approvals, and addressing regulatory concerns related to ingredients, claims, and product safety.

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