What is the first-time registration process for Chengdu professional pharmacists and what are the registration steps. What needs to be submitted for registration? I have compiled for you the first-time registration process for licensed pharmacists in Chengdu. I hope you like it! The first-time registration process for licensed pharmacists in Chengdu

Online login--gt; Fill in basic personal information online--gt; Online modification login Password--gt; Fill in the application form online--gt; Submit the application online--gt; Print the application form online--gt; Bring the review materials to the registration agency for review--gt; Check the review status online--gt; Register online Licensing Announcement--gt; Go to the registration agency to obtain the certificate for the first time registration of practicing pharmacists

1. Basis for approval

1. "The State Council sets administrative procedures for administrative approval items that really need to be retained" "Decision on Licensing" (State Council Order No. 412)

2. The State Food and Drug Administration's "Interim Measures for the Registration and Management of Licensed Pharmacists" (Guoyao Guanren [2000] No. 156)

3. "Supplementary Opinions on the Interim Measures for the Registration and Management of Practicing Pharmacists" (State Food and Drug Administration [2004] No. 342)

4. "Supplementary Opinions on the Interim Measures for the Registration and Management of Practicing Pharmacists" (Food and Drug Administration) Supervisor Letter [2008] No. 1)

5. "Notice on Revising and Issuing the Approval Procedure for Registration Management of Licensed Pharmacists" (Gan Food and Drug Supervisor [2007] No. 33)

2. Approval matters

First-time registration application for licensed pharmacist

3. Approval unit

Preliminary review: District and Municipal Food and Drug Administration

Acceptance: Provincial Drug Certification Center (Training Center)

Approval: Provincial Food and Drug Administration

IV. Conditions for approval

1. Obtain " Licensed Pharmacist Qualification Certificate";

2. Abide by laws and regulations, and abide by pharmacist professional ethics;

3. Be in good health and be able to persist in working as a licensed pharmacist;

4. With the consent of the practicing unit applying for registration;

5. Registration personnel should understand the relevant policies for practicing pharmacist registration and be able to submit registration applications through the Internet; prepare relevant materials as required and submit them within the prescribed time Registration application.

5. Time limit for review and approval

The total time limit for review and approval: 20 working days

Including: 5 working days for the district and city Food and Drug Administration

Provincial Drug Certification Center 9 working days

Provincial Food and Drug Administration 6 working days

6. Approval Procedure (1) Preliminary Review

1. Applicants should submit the following materials

(1) Electronic documents

Applicants log in to the (/) Licensed Pharmacist Network Service Platform and submit registration applications online.

(2) Paper materials

① "Application Form for First Registration of Licensed Pharmacist" in duplicate (print after completing the online application)

② "Practiced Pharmacist First Registration Application Form" Qualification Certificate" original and 1 copy; after the acceptance staff has verified that the original and copy are correct, the original will be returned to the applicant on the spot;

③ 1 copy of ID card;

④ The original and a copy of the physical examination form (within six months) from the disease prevention and control institution at or above the county level;

⑤ Proof of legal operation of the practice unit (drug production, business license or medical 1 copy of the institutional practice license);

⑥ 3 recent one-inch full-length color photos with the same bottom and front without hat;

⑦ 1 original and copy of the continuing education credit certificate for practicing pharmacists .

⑧When applying for registration, if the applicant is not a practicing pharmacist himself, he should submit a "Letter of Authorization";

2. Relevant requirements for application materials

(1) Application materials should be true, complete and clear, and all application materials should be on A4 paper. The copy should be completely consistent with the original, with the words "This copy is consistent with the original" marked, signed by the person in charge, and stamped with the official seal of the unit;

(2) "Application Form for Initial Registration of Licensed Pharmacist" Truthfully fill in the applicant's morality, ability, diligence, performance and any disciplinary violations in the assessment opinion column;

(3) The physical examination form for disease control institutions at the county level (inclusive) and above should be "Preventive Health Examination Form of the People's Republic of China - Health Examination Form for Practitioners" is valid only if it is stamped with the official seal of the physical examination institution and the results of the physical examination are recognized;

(4) Scope of practice It must be consistent with the business method in the legal business certificate;

(5) The practice category must be consistent with the professional category on the practicing pharmacist qualification certificate;

(6) The name of the practice unit must be consistent with the official seal and the name of the unit in the legal business certificate;

(7) After the applicant successfully applies online, the registration materials must be submitted to the local district and city Food and Drug Administration for preliminary review within 3 working days (online If the application takes more than 15 working days, the system will automatically delete the registration application information);

(8) Under normal circumstances, the 15th at the end of each quarter (March, June, September, December) The registration acceptance time for licensed pharmacists will be until the 20th, and the time will be postponed if there are holidays;

(9) Any licensed pharmacist who is a newly applied drug production and operating enterprise or an enterprise applying for GMP or GSP certification registers for the first time as a special To deal with the situation, you can submit application materials at any time (that is, during the non-quarterly acceptance time period, registration materials will be accepted due to special circumstances. If there is overlap with the quarterly acceptance time period, the application will be processed according to the approval time limit for quarterly acceptance). At this time, the registration application submitted by the applicant must not only have the human resources department of the district or city Food and Drug Administration where the applicant is located to sign the acceptance opinion and date in the remarks column, but also need to ask the drug circulation supervision department or the drug registration and safety supervision department to sign the acceptance opinion and date in the remarks column. Sign the company's application opinions, reasons and dates, and be signed by the person in charge and stamped with the official seal of the department. The time limit for approval refers to change and deregistration.

3. Review

Responsible unit for this position: Personnel Department of District Municipal Food and Drug Administration Job responsibilities and authorities:

Reviewers should review the application materials The authenticity, standardization and completeness of the materials shall be formally reviewed. For materials that meet the above requirements, the review manager shall sign the review opinions, signature, and stamp the official seal of the department, and then send them uniformly within 5 working days. Provincial Drug Certification Center; those who do not meet the requirements will return the materials to the applicant.

Working time limit: Complete within 5 working days (Submit to the Provincial Drug Certification Center on the 20th to 25th of March, June, September, and December, and the time will be postponed if there are holidays).

(2) Acceptance

Responsible unit for this position: Provincial Licensed Pharmacists Association

Job responsibilities and authorities: Provincial Drug Certification Center

Conduct a pre-acceptance formal review of the materials submitted by the Food and Drug Administration of each district and city, put forward acceptance opinions, sign online for materials that meet the requirements, issue an acceptance notice, and submit it to the leader in charge for signature; for unqualified materials The materials were returned to the district/municipal Food and Drug Administration and a notice of rejection was issued.

Working time limit: 5 working days (3 working days for the handling staff, 2 working days for the person in charge to sign and approve).

(3) Review

Person responsible for this position: Human Resources Department of Provincial Food and Drug Administration

Job responsibilities and authorities:

The acceptance materials submitted by the Provincial Drug Certification Center will be reviewed in accordance with regulations, review opinions will be put forward, and those that meet the requirements will be submitted to the person in charge of the department for review; those that do not meet the requirements will be returned to the Provincial Drug Certification Center.

Working time limit: 4 working days (2 working days for handling personnel, 2 working days for department heads).

(4) Approval

Person responsible for this position: Leader of the Provincial Food and Drug Administration Bureau

Job responsibilities and authority:

Review the approval opinions in accordance with regulations. If you agree with the review opinions, you will sign and approve the review materials and then transfer them to the Human Resources Office of the Provincial Food and Drug Administration; if you disagree with the review opinions, you will provide your review opinions and reasons, and return all materials to the Provincial Drug Certification Center through the original channels.

Working time limit: Within 2 working days.

(5) Certificate making and issuance

Responsible unit for this position: Provincial Drug Certification Center

Job responsibilities and authority: