The recently released IP 2010, which was originally scheduled to come into force from September 1, 2010, will now be implemented from December 1, 2010, according to the Scientific Body of the Indian Pharmacopoeia Commission (IPC) which met at Ghaziabad on August 20. This was done to accede to the request of IDMA and other professionals to give some time for study and implement the new standards.
“We will provide all support to the functioning and upgrading of IPC so that it can fulfil all the needs of the ensuring quality of medicines produced, sold and exported from India. India pharmacopoeia laboratory has also updating and creating a modern containerization facility to prepare and pack reference substances that are required while testing drugs. A few reference standards are already available for supply to the industry and all efforts are made to enhance this service in the next few months. IPC has its office and laboratory located at Ghaziabad in UP” said Dr G N Singh, Secretary cum Scientific Director of IPC.
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