Informative Notice
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Entry in the register of manufacturers of active substances
The manufacturer of active substances with head office in the Republic of Slovenia can start performing their activity after being entered in the register of manufacturers of active substances, managed by the relevant authority.
The register of manufacturers of active substances contains the following information:
- the name of the business entity and permanent address, contact data (telephone, fax, e-mail) and
- the manufactured active substance.
The competent authority issues a certificate upon entry into the register under the first paragraph.
The manufacturers of active substances notify their activity at the relevant authority at least 60 days before starting to perform the activity, i.e. on a written application that contains evidence on fulfilling the prescribed conditions and the list of active substances they intend to manufacture.
The competent authority enters the manufacturer of active substances in the register of manufacturers of active substances on the basis of a positive opinion of the expert commission for fulfilling the conditions for the manufacture of active substances in 90 or 60 days from the date of receipt of the complete application, if they assess that the verification of the fulfilment of conditions is not necessary.
If the expert commission under the previous paragraph issues a negative opinion on the fulfilment of conditions for manufacturing active substances, the competent authority rejects the entry in the register of active substances by issuing a decision.
Conditions
These terms apply to activity Production of active ingredients
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The manufacturer of medicinal products must ensure that production procedures are conducted in accordance with the principles and guidelines of good manufacturing practice. This provision also applies to medicinal products intended for export or removal from the market.
The principles and guidelines of good manufacturing practice include:
- A quality assurance system;
- appropriate staff;
- appropriate premises and equipment;
- suitable documentation;
- suitable production procedures;
- quality control;
- suitably arranged contract work;
- complaints, product recall and emergency unblinding;
- internal control;
- labelling of medicinal products for clinical trial;
- keeping records on medicinal products used in veterinary medicine -
Evidence
Certificate of good manufacturing practice
Legal basis
- Medicinal Products Act (ZZdr-2)
- Rules on conditions for completing activities of making medicinals and determining of conditions and procedure of publishing or revocation of execution good production practices
Competent Authority
Agency for Medicinal Products and Medical Devices of the Republic of Slovenia
Slovenčeva ulica 22
1000 Ljubljana
Procedures
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Entry in the register of manufacturers of active substances
Attachments
- Evidence of employment of sufficient number of experts with suitable education
- Evidence of availability of suitable premises, devices and equipment
- Evidence of pursuit of the activity in accordance with guidelines and principles of good manufacturing practice of active substances
Procedure costs
Administrative fee for the application and decision: 22.66 €