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Ensuring Safe Healthcare: The Comprehensive Approach of Our Pharmacovigilance Services

In today’s rapidly evolving healthcare landscape, ensuring the safety and efficacy of medicines is paramount. At SQNCE Life Sciences, we are dedicated to providing comprehensive pharmacovigilance services that prioritize patient safety while supporting the development and monitoring of pharmaceutical products throughout their lifecycle.

Our pharmacovigilance services encompass a wide range of activities aimed at detecting, assessing, understanding, and preventing adverse effects or any other drug-related problems. Here’s an overview of the key components of our approach:

  1. Adverse Event Reporting: We actively collect and document information on adverse events or reactions reported by healthcare professionals, patients, or other sources to promptly address potential safety concerns.
  2. Data Collection and Management: We utilize advanced data management systems to gather and organize data from various sources, including spontaneous reports, clinical trials, literature, and regulatory submissions, ensuring comprehensive oversight of safety information.
  3. Signal Detection: Our team employs sophisticated data analysis techniques to identify potential safety signals or emerging trends, allowing for proactive risk management and intervention.
  4. Risk Assessment and Evaluation: We conduct thorough risk assessments based on available data and scientific evidence to evaluate the potential risks associated with medicines and inform decision-making regarding their safe use.
  5. Risk Management: We collaborate with stakeholders to implement tailored risk minimization measures and optimize the benefit-risk profile of medicines, prioritizing patient safety at every stage.
  6. Pharmacovigilance in Clinical Trials: We adhere to rigorous pharmacovigilance standards in clinical trials to uphold ethical research practices and safeguard the well-being of study participants, maintaining the highest standards of safety and compliance.
  7. Post-Marketing Surveillance: Our vigilant post-marketing surveillance efforts enable us to monitor the safety of medicines after they have been approved and marketed, ensuring ongoing evaluation and management of safety risks.
  8. Safety Communication: We believe in transparent and proactive communication of safety information to healthcare professionals, regulatory agencies, patients, and the public, empowering informed decision-making and fostering trust in healthcare.
  9. Quality Assurance and Compliance: Our pharmacovigilance activities are conducted with meticulous attention to regulatory requirements and industry best practices, ensuring the quality, integrity, and reliability of our services.
  10. Collaboration and Networking: We actively engage with regulatory agencies, healthcare professionals, industry partners, and patient advocacy groups to foster collaboration and information sharing, advancing pharmacovigilance efforts and promoting collective efforts to enhance patient safety.

At SQNCE Life Sciences, we recognize the critical importance of pharmacovigilance in safeguarding public health and are committed to delivering exceptional services that meet the highest standards of safety, quality, and integrity. With our comprehensive approach and unwavering dedication to patient safety, we are proud to be a trusted partner in ensuring the safe and effective use of medicines for all.

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