Good Manufacturing Practices (GMP) terminology is mainly used in Pharmaceutical Industries. It is very important to maintain the process parameters, the right work environment for any manufacturing shop, in order to get the desired output. In spite of this, there is a possibility of the rejection or not getting the desired output. We come to know about the rejections or customer complaints only when they have happened. However, the risk assessment could be done for determining the possible risks during the manufacturing. 

Following the Good Manufacturing Practices can reduce the risks of rejection or rework during the manufacturing. There are ISO standards on GMP. Any new initiative in the organization starts with the awareness. The employees of the organization need to be made aware of or they need introduction of the new initiative. When organization decides to implement the GMPs, they should know what are GMPs. The strength of the ISO standards is, they are very clear about the requirements of a particular ISO standard. Sometimes the employees are capable of understanding the topic and even are equipped with the implementation tools, however only because they are not aware of the requirements, they are not able to proceed ahead for the implementation. Awareness is the first step towards continual improvement. 

One more advantage of conducting the common training is, the participants are able to compare and understand the commonalities as well as differences and unique requirements of all the standards. 

The implementors and auditors of IMS, generally have the confusion about how to integrate the systems including documentation, implementation, motoring and improvement as well as how to conduct the IMS audits in an integrated manner. 

The awareness course not only able to clarify all above doubts but also prepare the participants to face the IMS audits more courageously and effectively.