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3D Printing in Pharma 4 years after the first FDA approval: where are we now?23 to 24 May 2019 Antwerp, Belgium Course no. 6781Hot Topics Target group This course is organized for scientists and decision
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01
To fill out 3D printing in pharma, follow these steps:
02
Identify the specific pharmaceutical product or device that needs to be 3D printed.
03
Design a 3D model of the product using specialized software or hire a 3D designer.
04
Choose the appropriate materials for the 3D printing process, taking into consideration the requirements of the product.
05
Utilize a 3D printer capable of printing pharmaceutical-grade materials.
06
Set up the 3D printer according to the manufacturer's instructions and load the chosen materials.
07
Initiate the printing process and ensure that the printer is properly calibrated for accurate printing.
08
Monitor the printing progress and make any necessary adjustments to ensure quality and accuracy.
09
Once the printing is complete, remove the printed object from the printer and inspect it for any defects or imperfections.
10
Perform required post-processing steps, such as cleaning, sterilization, or additional treatments, depending on the intended use of the printed product.
11
Finally, package and label the 3D printed pharmaceutical product according to regulatory guidelines and standards.

Who needs 3d printing in pharma?

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Various stakeholders in the pharmaceutical industry can benefit from 3D printing technology, including:
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- Pharmaceutical companies: 3D printing allows for quicker and more cost-effective prototyping and production of customized drugs or medical devices.
03
- Doctors and medical professionals: 3D printing enables the creation of personalized medicine, tailored implants, and unique surgical tools.
04
- Patients: 3D printing can provide personalized medication dosages, individually designed prosthetics, and implants, improving patient outcomes and quality of life.
05
- Researchers: 3D printing aids in the development of new drug delivery systems, tissue engineering, and biomedical research.
06
- Regulatory authorities: 3D printing in pharma necessitates the establishment of guidelines and regulations to ensure quality, safety, and efficacy of printed products.
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3D printing in pharma refers to the use of additive manufacturing technology to create pharmaceutical products, such as pills or implants, in a more personalized and efficient way.
Pharmaceutical companies, research institutions, and regulatory bodies may be required to file information related to 3D printing in pharma.
To fill out information related to 3D printing in pharma, stakeholders must provide details on the technology used, type of product produced, intended use, and any regulatory approvals.
The purpose of 3D printing in pharma is to enable personalized medicine, improve drug delivery systems, and accelerate the development of new pharmaceutical products.
Information that must be reported on 3D printing in pharma includes details on the technology, product specifications, regulatory compliance, and any adverse events or quality control issues.
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