Can anyone give me the complete set of GMP Material Management Standards and Material Management Ope

If you look for more, you will have it.

Legal Analysis:1Strictly check whether the transportation quantity is consistent with the number of notification reports, and carry out acceptance on a vehicle-by-vehicle basis.

2.It should be sorted and stacked, and the sign should be listed.

3.Where the transport vehicle does not obey the command, parked indiscriminately, can refuse to sign.

4.Conscientiously do a good job of original records such as warehousing registration forms and ledgers, and timely and accurately report the latest forms and monthly reports.

legal basis; Civil Code of the People's Republic of China

Article 707: Where the lease period is more than six months, it shall be in writing. If the parties do not use the written form, it is impossible to confirm Article 707 If the lease term is more than six months, the written form shall be cancelled. If the parties do not adopt written form and cannot determine the term of the lease, it shall be deemed to be an indefinite lease.

If the lease term is fixed, it shall be regarded as an indefinite lease.

Article 710 The lessee shall not be liable for compensation if the leased property is used in accordance with the agreed method or according to the nature of the leased property, resulting in the loss of the leased property.

Article 715 The lessee may, with the consent of the lessor, make improvements to the leased property or add other things. If the lessee improves or adds other things to the leased property without the consent of the lessor, the lessor may request the lessee to restore the original state or compensate for the loss.

According to GMP, materials do not include semi-finished products.

The details of GMP are as follows:

GMP is an abbreviation for good manufacturing practice, which Chinese means "Good Manufacturing Practice". The World Health Organization defines GMP as a regulation that guides the production and quality management of food, drugs, and medical products.

GMP is a set of mandatory standards applicable to the pharmaceutical, food and other industries, requiring enterprises to meet the health and quality requirements in accordance with the relevant national laws and regulations in terms of raw materials, personnel, facilities and equipment, production process, packaging and transportation, quality control, etc., and form a set of operable operating specifications to help enterprises improve the sanitary environment of enterprises, find problems in the production process in time, and improve them.

On July 11, 1995, the Ministry of Health of the People's Republic of China issued Wei Yao Fa (1995) No. 35"Notice on carrying out drug GMP certification"。Drug GMP certification is a system in which the state implements GMP supervision and inspection of drug manufacturers (workshops) and drug varieties in accordance with the law and obtains recognition.

Drug GMP certification is divided into national and provincial levels, according to the provisions of the "Regulations on the Implementation of the Drug Administration Law of the People's Republic of China", the provincial level or above the people's drug regulatory department shall be in accordance with the "Good Manufacturing Practice for Drugs" and the implementation measures and implementation steps stipulated by the drug regulatory department, organize the certification of drug manufacturers.