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SPECIAL ACCESS PROGRAMME PRODUCTS ORDER FORMALL ORDERS MUST BE FAXED Site:Hospital/Customer:Phone /Fax:City/Town:Date:Time:Requested By: Routine Delivery Priority:ASAP *STAT [*STAT orders must be
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How to fill out special access programme products

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How to fill out special access programme products

01
Access the official website of the special access program.
02
Navigate to the section dedicated to special access program products.
03
Download the application form specific to the products you need.
04
Fill out the form with accurate personal and healthcare information.
05
Include any necessary documentation or medical records that support your request.
06
Review your application for completeness and accuracy.
07
Submit the application through the designated online portal or send it to the specified mailing address.

Who needs special access programme products?

01
Patients with conditions not adequately treated by available therapies.
02
Healthcare providers seeking access to innovative medications for their patients.
03
Individuals participating in clinical trials who require additional support.
04
Researchers looking to study specific products under the special access program.
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Special access programme products refer to medical products that are available for patients who have serious or life-threatening conditions and for whom no comparable alternative therapies are available. This allows for expanded access to investigational drugs, biological products, and medical devices.
Manufacturers and sponsors of investigational products seeking approval for use outside of clinical trials are required to file special access programme products.
To fill out special access programme products, applicants must complete the required forms outlining patient information, product details, the rationale for access, and any necessary clinical data to support the request.
The purpose of special access programme products is to provide patients with access to unapproved medical products that may be necessary for their treatment when no satisfactory alternatives exist.
Information that must be reported includes the patient's medical history, the specific product being requested, dosage information, treatment protocols, and any potential risks associated with the use of the product.
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