Yes, our regulatory consulting team is well-versed in global and local regulatory requirements and can assist in submissions across various countries, ensuring compliance with respective authorities.

Pharmacovigilance involves monitoring and assessing the safety of pharmaceutical products throughout their lifecycle. It is crucial for detecting, evaluating, and preventing adverse effects or any other drug-related problems.

There are currently no job opportunities available. pleaseregularly check our website for job postings soon.

We offer a comprehensive range of services including pharmacovigilance, clinical trial design and management, regulatory consulting, data management and statistical analysis, as well as medical writing and scientific editing.

Our experts provide precise and compliant documentation, including scientific papers, regulatory submissions, and other critical documents, ensuring clarity, accuracy, and adherence to industry standards.

Our team comprisesof experienced professionals with subject matter expertise who meticulously review and edit documents, adhering to industry standards and regulatory guidelines.

We employ advanced data management systems and statistical software to handle diverse datasets efficiently, ensuring accurate analysis and meaningful interpretations.

Regulatory consulting involves navigating complex regulations to ensure compliance with local and global standards. Our servicesassist in preparing andsubmitting regulatory documents,facilitating approvals for drug development and marketing.

Our pharmacovigilance service includes adverse event reporting, signal detection, risk management, label review, Qualified Person for Pharmacovigilance (QPPV),Audits and Inspection, Literature surveillance, Case reporting,and periodic safety updates required for regulatory compliance.

Yes. Internship opportunities are available.Please contact us for further information.