Translation of "cost goods manufactured " (English → French) :

manufacturing statement [ cost of goods manufactured statement | cost of goods manufactured schedule ]

plan leather goods production | plan leatherwear manufacturing | plan leather goods manufacture | plan leather goods manufacturing

building of daily use goods | daily use goods manufacturing | construction of daily use goods | manufacturing of daily use goods

apply methods for footwear and leather goods production | apply methods for leather goods manufacturing | apply methods for footwear and leather goods manufacturing | organise technical operations for footwear and leather goods production

cost of goods manufactured

manufacturing statement | cost of goods manufactured schedule

cost of goods manufactured

good manufacturing practices | GMP | good practices | good manufacturing practice

manufactured goods [ manufactured products | manufactures ]

Guide to good manufacturing practice for medicinal products

A harmonised regulatory framework at Union rather than at Member State level reduces costs for manufacturers, ensures a level playing field and ensures the free movement of goods across the internal market.

In the area of trade in goods, differences in regulations can create hurdles for market access since they may cause additional costs for manufacturers, for example where products must be tested by independent laboratories and certified in the target market before they can be sold, or special versions of products must be developed to comply with detailed technical regulations.

In the area of trade in goods, differences in regulations can create hurdles for market access since they may cause additional costs for manufacturers, for example where products must be tested by independent laboratories and certified in the target market before they can be sold, or special versions of products must be developed to comply with detailed technical regulations.

A centralised marketing authorisation procedure, to benefit from the pooling of expertise at European level and direct access to the EU market; A new and multidisciplinary expert Committee (Committee for Advanced Therapies), within the European Medicines Agency (EMEA), to assess advanced therapy products and follow scientific developments in the field; Tailored technical requirements, which are adapted to the particular scientific characteristics of these products; Detailed guidance for the application of good manufacturing practice and good clinical practice to advanced therapies; Strengthened requirements for risk management and po ...[+++]st-authorisation traceability; A system of low-cost, top-quality scientific advice for the industry, provided by the European Medicines Agency; Financial and administrative incentives for small and medium-sized enterprises developing advanced therapies.