Licenses library · 369

Licensing Pharmacist to establish Drug and Medical Product Factory

药师开办药品及医疗产品工厂许可

ໃບອະນຸຍາດວິຊາຊີບເພສັດຊະກໍາ ເພື່ອສ້າງຕັ້ງໂຮງງານຜະລິດຢາ ແລະ ຜະລິດຕະພັນການແພດ

Individuals or organizations that intend to produce drugs and medical products must first obtain the approval and technical permission from the Ministry of Health. Apply at Food and Drugs Department.

Who needs this

Individuals or organizations that intend to produce drugs and medical products must first obtain the approval and technical permission from the Ministry of Health.

Requirements

  1. A full-time pharmacist that has at least five years of experiences
  2. Never been sanction on drugs or narcotics or medical products
  3. Has a pharmacological and business ethics
  4. Has skilled human resources
  5. Healthy, no mental illness or contracted transmissible diseases
  6. Has a safety and environmental protection measures
  7. Has a suitable site and necessary infrastructures, has a standard warehouse and transport vehicle. Factory must have a manufacturing room, laboratory with full sets of equipment.

Documents — first application

Document Note
Application Form 1 copy
Education Certificate 1 copy
Retirement Card or Resignation Letter or Certificate of Resignation from Public Servant or Appointment Certificate from Organization (if it is a state-enterprise), 1 copy
Photo (3x4) 1 photo (taken within 1 year)
Location Map of the Factory 1 copy
Site Plans of the Factory 1 copy
Certificate of Nationality for an alien. - for a foreigner, it is required to have related certification and permits according to the regulations of the Lao PDR
Copy of Enterprise Registration Certificate 1 copy
Feasibility Study of Medical and Medical Devices Business includes the product information, materials, origins, and other related technical information. 1 copy
Certificate of Pharmacist Practices 1 copy
Certificate of Ownership of the House or Lease Agreement, 1 copy
Certification of Health issued within 3 months, 1 copy
Address Certification taken within 3 months, 1 copy
Report for the location inspection issued by the FDD authority, 1 copy
Curriculum vate with photo (taken within 1 year), 1 copy
Court Clearence 1 copy

Documents — renewal

Document Note
Application form for renewal This application is required to receive official comments from the District Office of Health and Provincial Department of Health before sending to the Food and Drug Department, Ministry of Health for its consideration and approval.
Certification of Health 1 copy
Address Certification 1 copy
Performance report and 1-year future plan
Licensing Pharmacist original copy
Report for the location inspection issued by the FDD authority, with evidence on importing raw materials and packaging tools, 6 copies

How to submit

Address of authority
Food and Drugs Department, Ministry of Public Health
Processing time
45 The application processing period is within 45 days

Validity and renewal

Has an expiry date
YES
Validity
36 months
Renewal process
Licensing Pharmacist is valid for 3 years. 3 months before the date of expiry, the business must apply for a renewal. (Article 6, Instructions on the Drugs and Medical Products Manufacturing No. 937/MOH, 12.05.2004). Food and Drug Department is in charge of the license approval after the application got approved through the relevant authorities at the district, provincial-capital levels. The conditions for license renewal are related to Section III, Section IV of the Instructions on Drugs and Medical Products Manufacturing No. 937/MOH, 15.05.2004 and other relevant regulations. Conditions for non-renewal are stipulated in Article 6.3 (Instructions on the Drugs and Medical Products Manufacturing No. 937/MOH, 12.05.2004). Temporary suspension or termination of the business operation is subjected to: -Death of the pharmacist. -In case of warning and have been fined more than 3 times - In case of misconduct or violation of the Laws - Has been filed a lawsuit by the affected people and the victims or prosecuted by the court

Additional comment

Article 4. Conditions on the settings of Drug and Medical products factory (Instructions on Drug and Medical Product Manufacturing 937/MoH 12/05/2004)

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