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ProcedureEdit
Apply In-Person:
- Application form for obtaining pharmaceutical manufacturing permit in Tanzania is available in Tanzania Medicines and Medical Devices Authority contact link
- Applicant must provide all information that is necessary in the application form.
- Applicant should make sure to carry photocopies and originals of documents that are necessary for completing this procedure.
- Documents that are needed for completing this procedure are mentioned under “Required Documents” section of this page.
- Applicant must attach photocopies of all documents (whichever is necessary) along with the application form while submitting the form at the office.
- Fee for this procedure is listed in detail under “Fees” section of this page.
- If all the above-mentioned procedures were followed properly by the applicant, an inspection date will be fixed by concerned authorities.
- During the date of inspection, the applicant must be present at the office premises for explaining about various manufacturing details in the premises to the inspection officer.
- Once the applicant passes the inspection test, they will be notified regarding their permit availability within 21 days.
- If there is no information regarding the permit is provided, applicant can visit the office to know status of their application.
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Required DocumentsEdit
- Certificate of Incentives
- Memorandum
- Environmental Clearance Certificate
- Scoping report approval letter
- Plan layout
- TFDA Invoice
- Bank Slip
- TFDA Receipts
Office Locations & ContactsEdit
Tanzania Medicines and Medical Devices Authority
Location: Dar es Salaam
Address:
TMDA HQ, Nelson Mandela Rd,
Dar es Salaam,
Tanzania
Contact: (+255) 222450512
Contact link
Location link
EligibilityEdit
- Any individual who is willing to engage in Pharmaceutical manufacturing business in Tanzania are eligible.
FeesEdit
- TZS 700,000 for Business permit fee of a large pharmaceutical factory.
- TZS 150,000 for Good manufacturing practice GMP Inspection fee per year.
- TZS 6,926,710.91 for Good manufacturing practice GMP inspection for facilities within the East African Region.
- TZS 577,225 for GMP inspection fee for domestic / local pharmaceutical manufacturing plant.
ValidityEdit
- The permit is valid for 1 year.
Documents to UseEdit
Please attach documents that can be used by people. e.g. links
Sample DocumentsEdit
Please attach sample completed documents that would help other people.
Processing TimeEdit
- The processing time for this procedure is within 21 days.
Related VideosEdit
Videos explaining the procedure or to fill the applications. Attach videos using the following tag <&video type='website'>video ID|width|height<&/video&> from external websites. Please remove the '&' inside the tags during implementation. Website = allocine, blip, dailymotion, facebook, gametrailers, googlevideo, html5, metacafe, myspace, revver, sevenload, viddler, vimeo, youku, youtube width = 560, height = 340, Video ID = Can be obtained from the URL of webpage where the video is displayed. e.g In the following url 'http://www.youtube.com/watch?v=Y0US7oR_t3M' Video ID is 'Y0US7oR_t3M'.
InstructionsEdit
- Applicant must provide genuine information while applying for this procedure.
- Applicant should make sure to follow all instructions as mentioned by concerned authorities properly.
Required InformationEdit
- Full Name
- Date of Birth
- Business Premises Address
- Amount Invested
- Source of the Manufacturer
- Signature
Need for the DocumentEdit
- This permit is necessary for manufacturing pharmaceutical products in Tanzania.
Information which might helpEdit
- Tanzania Medicines and Medical Devices Authority (TMDA) is responsible for providing licenses and permits for medical manufacturers in Tanzania.
Other uses of the Document/CertificateEdit
Please explain what are other uses of obtaining this document/certificate. e.g. Birth Certificate can be used as proof of identity.
External LinksEdit
- Tanzania Medicines and Medical Devices Authority (TMDA) link
OthersEdit
More information which might help