The way to success for pharmaceutical enterprises: from safety to quality

In recent years, with the development of social economy and the increase of people's attention to health, the demand and supply of drugs and health food have increased dramatically, and the safety of drugs has become increasingly prominent In the view of the insiders, to truly grasp the dual attributes of "security" - Security and "sense of security" is the way to success for a pharmaceutical enterprise Product incubation period: set strict standards According to the industry, setting strict standards at the initial stage of product incubation is a high-quality innate essential gene Taking Chinese herbal medicine as an example, Chinese herbal medicine is the source of traditional Chinese medicine production Strengthening the source management of Chinese herbal medicine and Chinese herbal pieces is of great significance to ensure the quality and safety of traditional Chinese medicine production In recent years, with the prominent problems in the field of source management of traditional Chinese medicine (decoction pieces), such as adulteration makes fake, inferior and so on, the food and drug regulatory departments around China continue to strengthen the management of traditional Chinese medicine (decoction pieces) in the production of traditional Chinese medicine In this regard, some traditional Chinese medicine manufacturers have set strict standards, strengthened their own supervision and inspection, carried out the quality management of traditional Chinese medicine production in strict accordance with the requirements of GMP, strictly controlled the source and inspection, and put an end to the use of fake and inferior traditional Chinese medicine, non-medical parts of traditional Chinese medicine and polluted or extracted traditional Chinese medicine to produce herbal pieces Product production period: quality control is required As far as drugs are concerned, safety takes the first place However, incidents exposed due to drug safety problems still occur frequently For example, in recent years, there have been many false events in vaccine production records, which shows that some pharmaceutical enterprises have weak risk awareness, and they still have a fluke mentality for GMP based standardized production According to GMP, the production records of pharmaceutical enterprises must include product name, specification, batch number, date and time of start and end of production and intermediate process, signature of person in charge of each production process, abnormal event report, etc Therefore, if the pharmaceutical enterprises want to build up the public's trust in products, they must do every step carefully and steadily to achieve the controllable product quality In order to save cost and time, they must not fabricate and tamper with the production records, so as not to cause defects in product quality This also shows the importance of scientific management and production of employees Product storage period: depending on the relevant equipment, the industry said that the safety of drugs will change with the change of the environment Therefore, we need related high-tech equipment to ensure the safety of products In terms of the temperature range of the medicine, the medicine is kept at 10 ℃ - 30 ℃, under 20 ℃ in the shade and 2 ℃ - 8 ℃ in the cold storage If the temperature exceeds the standard, the drug is prone to deterioration, mildew, moth eaten, failure, etc., which affects the safety of patients For example, in the hot summer, in order to ensure that the medicine is in a relatively safe environment, a special cool room or refrigerator should be prepared in the general pharmacy, such as snake gall orange peel liquid, paediatric paracetamol Huang Namin granules, vitamin AD drops, etc., which can exist in a cool area, and the temperature should be controlled below 20 ℃ Generally speaking, in product development, process production, customer service, environmental protection and other links, only by implementing the quality management philosophy of "pursuit" to the end and strictly controlling "zero defect" quality over pharmaceutical standards in the whole process, can we ensure the quality and safety of drugs and realize the evolution from "manufacturing" to "quality".