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(Grp) good radiopharmaceutical practice
1.
2. GRP means GMP applied to radiopharmaceuticals
because of special nature of these products. The
GRP are the guidelines designed , documented
and implemented for the protection of workers,
patients and preparation of safe
radiopharmaceutical.
3. By following GRP the quality built into:
1) Process preparation
2) Administered to patient
3) QC testing
4. GRP CONCERNS
with :
1) Personnel
2) Premises & equipments
3) Preparation
PERSONNEL :
All personnel employed in areas where radioactive products are manufactured should be
qualified.
5. PREMISES & EQUIPMENTS :
GRP requirements for radio pharmacy are:
1) Design and location of radio
pharmacy
2) Minimal access to public
and patient
6. 3) Protect the product against
environmental contamination
4) Clean and disinfected surface