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On February 18, the CFDA announced the latest phase of the GMP certification for pharmaceuticals. 65 pharmaceutical manufacturing companies such as Shandong New Times Pharmaceutical Co., Ltd. passed GMP on-site inspections, and the number of GMP certified companies in China increased to 861.
At present, some domestic companies are busy with large-scale mergers and acquisitions, while another part of the company hastened to dispose of non-core assets and light vehicles to hurry.
For example, in recent years, Dazhong Pharmaceutical Co., Ltd. has sneezed around the globe and its GPIC Group, which has always focused on internal reforms, has finally expressed its expansion ambitions. It said that it will use the opportunity for the expiration of the new GMP certification to acquire 20 to 30 companies in 3 to 4 years. Pharmaceutical companies, with injections and biopharmaceuticals as their main targets, will concentrate their efforts on production approvals and mergers and acquisitions of industrial companies. Currently, they are negotiating with more than a dozen companies; Yabao Pharmaceuticals has announced that it will not pass new GMP standards. Company Yabao North Zhongda Company sells.
According to Wang Weibing, an expert member of the GMP design group and deputy general manager of Zhejiang Hisun Pharmaceutical, the company’s acquisition is mainly related to the company's development strategy. At present, it still targets product approvals, but the original production is not full, transformation and new investment and production. It is of little significance for products that are out of proportion to one another to continue to reinvest huge sums of money in a relatively overcapacity environment, or if the product area is not a product of strategic development of the company, it will take this opportunity to make adjustments.
However, Wang Weibing also pointed out that the status quo of relatively overcapacity will not change significantly due to the implementation of new GMP, and competition in the industry will remain fierce.
“A more effective measure is the liberalization of the licensing policy for marketing licenses and production licenses. This will more effectively stimulate the industry to revitalize assets and accelerate the phase-out of the industry. This is a strong appeal for the industry and hopes that the “Drug Administration Law†is being amended. There will be a breakthrough in the listing licensor system,†Wang Weibing said.
2. Size: The size of pavement sign boards can vary depending on their intended use. They typically range from 18 inches to 36 inches in width and 24 inches to 48 inches in height.
3. Weight: The weight of pavement sign boards can vary based on the material used. Aluminum sign boards are lightweight, while steel and plastic sign boards can be heavier.
4. Shape: Pavement sign boards are typically rectangular in shape, but can also be square or circular.
5. Graphics: Pavement sign boards can be printed with graphics or text on one or both sides. Graphics can be printed using a variety of methods, including vinyl graphics, digital printing, or screen printing.
6. Frame: Pavement sign boards may have a frame that holds the sign in place and provides stability. Frames can be made of the same material as the sign board or can be a different material.
7. Base: The base of pavement sign boards can be weighted to provide stability in windy conditions. Some pavement sign boards have a water-filled base, while others have a sand-filled base.
8. Weather resistance: Pavement sign boards are designed to withstand outdoor weather conditions, such as rain, wind, and sunlight. Some sign boards are treated with UV-resistant coatings to prevent fading.
9. Portability: Many pavement sign boards are designed to be portable, with wheels or a handle for easy transport. This makes them ideal for businesses that need to move their signage around frequently.
Overcapacity will not change significantly due to new GMP implementation
According to the relevant announcement of the State Food and Drug Administration (CFDA), enterprises that have passed certification can basically guarantee the market demand for sterile medicine in China. The new GMP requirements for injections have increased. It is indeed a relatively big challenge for companies that are not fully productive, have poor production equipment, and have insufficient strength.