1964_PHARMACY_AND_POISONS_REGULATIONS — Page 65

HK Historical Laws 香港歷史法例 All AI Reviewed

1987 Ed.]

Pharmacy and Poisons Regulations

[CAP. 138

A 65

[Subsidiary]

FORM 3

[reg.29(5).]

表格三

[規例第二九條第(五)款]

PHARMACY AND POISONS ORDINANCE 藥劑及毒藥條例

(Chapter 138)

(香港法例第一三八章)

CERTIFICATE FOR MANUFACTURER

It is hereby certified that

茲證明

製造商證明書

(Name of the pharmaceutical firm)

(製藥廠名稱)

(1) is authorized to manufacture and market drugs and pharmaceutical products;

已獲准製造及銷售藥物及藥劑製品;

(2) is subject to regular inspections which have shown that it follows the requirements of good practices in manufacture and quality control of drugs and pharmaceutical products as recommended by the World Health Organization, and is included in the list established for that purpose.

經常受到檢查,並經證明已依照世界衛生組織之建議,在藥物及藥劑製品之製造及品質管制方面,遵循其所規定之良好習慣。該製藥廠已列名於爲此而設之名單內。

HONG KONG.

香港

(Date)

日期:

藥劑業及毒藥管理局

for Pharmacy and Poisons Board.

代行

Page 65


Page 66

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1987 Ed.] Pharmacy and Poisons Regulations [CAP. 138 A 65 [Subsidiary] FORM 3 [reg.29(5).] 表格三 [規例第二九條第(五)款] PHARMACY AND POISONS ORDINANCE 藥劑及毒藥條例 (Chapter 138) (香港法例第一三八章) CERTIFICATE FOR MANUFACTURER It is hereby certified that 茲證明 製造商證明書 (Name of the pharmaceutical firm) (製藥廠名稱) (1) is authorized to manufacture and market drugs and pharmaceutical products; 已獲准製造及銷售藥物及藥劑製品; (2) is subject to regular inspections which have shown that it follows the requirements of good practices in manufacture and quality control of drugs and pharmaceutical products as recommended by the World Health Organization, and is included in the list established for that purpose. 經常受到檢查,並經證明已依照世界衛生組織之建議,在藥物及藥劑製品之製造及品質管制方面,遵循其所規定之良好習慣。該製藥廠已列名於爲此而設之名單內。 HONG KONG. 香港 (Date) 日期: 藥劑業及毒藥管理局 for Pharmacy and Poisons Board. 代行 Page 65 Page 66
Baseline (Original)
1987 Ed.] Pharmacy and Poisons Regulations [CAP. 138 A 65 [Subsidiary] FORM 3 [reg.29(5).] 表格三 [規例第二九條第(五)款 PHARMACY AND POISONS ORDINANCE 藥劑及毒藥條例 (Chapter 138) (香港法例第一三八章) CERTIFICATE FOR MANUFACTURER It is hereby certified that 茲證明 製造商證明書 (Name of the pharmaceutical firm) (製藥廠名稱) (1) is authorized to manufacture and market drugs and pharmaceutical 准製 製造及銷售藥 物及藥劑 products; 製品; (2) is subject to regular inspections which have shown that it follows the 經常受到檢查,並經證明已依照世界衛 requirements of good practices in manufacture and quality control of 生組織之建議,在藥物及藥劑製品之製 drugs and pharmaceutical products as recommended by the World 造及品質管制方面, 遵循其所規定之良 Health Organization, and is included in the list established for that 好習慣。該製藥廠已列名於爲此而設之 purpose. 名單內。 HONG KONG. 香港 (Date) 日期: 藥劑業及毒藥管理局 for Pharmacy and Poisons Board. 代行 Page 65Page 66
2026-05-05 05:20:35 · Baseline
View content

1987 Ed.]

Pharmacy and Poisons Regulations

[CAP. 138

A 65

[Subsidiary]

FORM 3

[reg.29(5).]

表格三

[規例第二九條第(五)款

PHARMACY AND POISONS ORDINANCE 藥劑及毒藥條例

(Chapter 138)

(香港法例第一三八章)

CERTIFICATE FOR MANUFACTURER

It is hereby certified that

茲證明

製造商證明書

(Name of the pharmaceutical firm)

(製藥廠名稱)

(1) is authorized to manufacture and market drugs and pharmaceutical 已 獲 准製 製造及銷售藥 物及藥劑

products;

製品;

(2) is subject to regular inspections which have shown that it follows the 經常受到檢查,並經證明已依照世界衛

requirements of good practices in manufacture and quality control of 生組織之建議,在藥物及藥劑製品之製 drugs and pharmaceutical products as recommended by the World 造及品質管制方面, 遵循其所規定之良

Health Organization, and is included in the list established for that 好習慣。該製藥廠已列名於爲此而設之

purpose.

名單內。

HONG KONG.

香港

(Date)

日期:

藥劑業及毒藥管理局

for Pharmacy and Poisons Board.

代行

Page 65Page 66

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