As ALBE Law and Consultancy, we provide all kinds of legal services our clients need in the field of Health and Pharmaceutical Law through our personal experience in this field and our expert consultants in the sector. The main services we offer to our customers are:
- Providing consultancy services in malpractice compensation cases arising from physician practices and in cases where physicians' legal and criminal responsibilities may come to the fore, and acting as a party representative in legal disputes,
- Preparation of purchase-sale agreements and pharmaceutical production-development agreements regarding pharmaceutical raw materials,
- Preparation of contracts regarding distributorship and clinical research,
- Providing legal services regarding the liability of healthcare personnel arising from medical errors and the rights of patients and physicians,
- Providing consultancy services regarding Ministry of Health permit procedures,
- Following up of cases regarding disputes arising from pharmaceutical patents and pharmaceutical brands,
- Carrying out administrative application processes regarding the reimbursement of drugs that are not covered by the social security institution and resolving legal disputes that may arise subsequently.
- Providing consultancy activities in administrative processes regarding off-label drug use practices.
- Providing consultancy services regarding the collection of expenses related to cancer drugs from the social security institution and managing the processes related to legal disputes.
In addition to these services, we provide services to companies operating in the sector through our sector expert consultants with whom we cooperate;
- Conducting consultancy activities in areas such as health economics, market research, drug pricing and market access, providing support to pharmaceutical companies on drug pricing and marketing,
- Conducting market research to help customer companies follow the trends and opportunities in the sector,
- Communicating with the authorities in the process starting from the registration process of the drug until it is put into use, preparing the necessary files, making applications and following the process after the drug is put into use,
- Making drug pricing at reasonable prices, the rules of which are determined by the Ministry of Health, and monitoring the changes in these prices in the light of the legislation,
- Following up applications for the corporate relations process, holding meetings with decision makers and creating follow-up processes after alternative repayment approval.
- Required studies to add drugs to foreign drug lists, prepare files and support the processes after the product is added to the foreign drug list.
- To carry out the project process regarding all public institutions and organizations upon request.
