India's Leading Regulatory and Registration Service provider.CPPL is known for it's expertise in writing Dossier,DMF,CTD,ACTD,eCTD,EU CTD,US DMF,EU DMF,KDMF and compilation of all kind of registration files and submission of the same query support.
CPPL believes GMP must not be in percentage It must be 100%.CPPL supports for Plant Setup,Quality System Setup,Quality Assurance Documentation,Regulatory Audits,Validation services,Quality system integration,GMP Training and Evaluation.
We impart training with 100% practical approach. CPPL Trainers are well known in industry for their knowledge,communication skill and their training skill.We make the technocrats with our training.CPPL Belives best training puts best quality in product.
CPPL developed eCTD Conversion software which is leading to reduce down cost of our Services.CPPL Converts eCTD in lowest cost,completely validated and compliant with regulatory submission gateways.CPPL also have expertise in submission of eCTD files to Regulatory authority
First concept of India for Certification of Pharmaceutical Industry.We refers a guideline which is blend of almost all guidelines of world leading regulatory authorities CPPL provides gradation with certificate.CPPL have 30 leading senior auditors on it's auditors panel.
CPPL knows about the requirements of authorities related to BA BE and clinical studies,we are known for sourcing genuine studies from our associate CRO Centers,we are your mediator for review,you may get studies from CRO but it needs to be checked before submission .