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GSP pharmacy refrigerator temperature and humidity form how to do

As shown:

Specifically as follows:

I. Basic requirements?

1, unified with a black water-based pen to fill out.?

2, the record shall not be altered, pasted, and shall not leave blank lines.?

3, the record is filled in line by line, no apostrophe.

4, the record is wrong, with a straightedge to draw a horizontal line (red) and next to the date of correction and correction of the person's name, another line to refill the correct content.

5, each record should be added to the company's unified printing of the special cover, fixed with a plastic pole clip into the data box for inspection.

6, the record cover should be filled with the name of the record and start date.

Temperature and humidity records?

1, fill in the store name and month before recording.

2, manually fill in the appropriate temperature range.?

3, business room: 0 ~ 30 ℃; freezer: 2 ~ 8 ℃?

4, suitable relative humidity range 35 ﹪ ~ 75 ﹪?

5, every day 9:00 am to 10:00 pm, 3:00 pm to 4:00 pm to fill out a record, each record should be signed in time.

6, control measures should be regulated to the appropriate range of temperature and humidity data to fill in again.

Three, conservation equipment use and maintenance records?

1, summer start time from 9:00 a.m., until about 21:00 p.m. until the middle of the time depending on the situation (room temperature drops below 26 ℃) shutdown.

2, relative humidity reaches or exceeds 75 ﹪, ventilation or air conditioning method of dehumidification.

3, the room temperature reaches or exceeds 8 ℃, biological products and other drugs need to be preserved within 2 ℃ ~ 8 ℃ should be placed in a refrigerator sealed preservation (such as: human albumin injection, human immunoglobulin, Novalbumin 30R refill, insulin preparations, recombinant human interferon α-2b gel, etc.).

4, room temperature reaches or exceeds 25 ℃, need to 25 ℃ below the preservation of drugs should be placed in a refrigerator sealed preservation, such as: ursine injection; BCG polysaccharide ribonucleic acid injection / Skikon injection; atorvastatin tablets / ALE; felodipine sustained-release tablets / Boyd's; diclofenac sodium double-release enteric capsules / Dyfen capsule; deoxyprogesterone ethinyl estradiol tablets / Momoflower; akaposan tablets / Bayerisin tablets; mometasone furoate ointment/Elosone fluvastatin capsules/Lysol capsules; aspirin vitamin C effervescent tablets/Bay Aspirin, etc.?

5, fill in the following should be marked: store name, equipment name, specification model, equipment number, year, etc.?

6, air conditioning, refrigerated cabinets (no drugs) is not in use, maintain cleanliness and hygiene, to maintain the state of being enabled at any time, by the monthly trial, make a record.?

Four, drug maintenance records, Chinese medicine tablets maintenance records?

1, the display of drugs on a monthly basis.

2, near the expiration date of the drugs, easy to mold, easy to dampen the drugs, split drugs, refrigerated drugs as a key maintenance varieties, regular monthly maintenance records (can be focused on the 26th of each month to fill out).

3, summer (June to September) will be suppositories, ointments, syrups and other drugs susceptible to temperature as a key maintenance varieties of maintenance.?

4, the storage of drugs found to have quality doubts, should be immediately removed from the cabinet, stop selling, fill out the "quality query report form" (in duplicate), reported to the quality control department for processing.?

5, the following drugs should be described in the Remarks column: varieties with an expiration date of less than six months, split drugs, drugs stored in refrigerated cabinets, and other drugs that need to be checked.