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Opt for efficiency and value implement our solutions to streamline your clinical development and maximize your product’s impact.
KLCRO provides strong bridge of communication and provision of regulatory services for clinical trial of sponsor’s product as per global clinical research protocols such as “GCP Guidelines” and “Biostudy rules alinged with DRAP ACT 2012”.
KLCRO has a diverse team of qualified professionals including physicians, pharmacists, medical professional, content writers, IT experts, biostatisticians and clinical research associates working collaboratively with CTUs to provide clinical research services during a whole clinical trial project. We have all the top CTUs on the board in all the major cities of Pakistan to fulfill the sponsor’s study protocol criteria by strictly following our health ministry standards.