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Why Altrid
Our Mission Empowering progress through innovation and excellence
At the intersection of clinical science and data analytics, our Clinical Research Organization (CRO) stands as a dynamic partner for pharmaceutical and biotechnology industries seeking excellence in clinical data analysis.
We specialize in converting complex clinical trial data into regulatory-ready submission packages and actionable intelligence through our versatile, flexible and cost effective service solutions.
Our Vision Create innovative solutions that drive lasting positive change
We play a crucial role in helping pharmaceutical, biotech and research organizations navigate the complexities of clinical trials data analysis and regulatory compliance.
By transforming raw clinical information into strategic insights, we empower our clients to make evidence-based decisions that accelerate drug development timelines, enhance submission quality and ultimately improve patient outcomes.
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OUR STRATEGY Delivering Excellence in Data Organization
Our team's deep expertise enables our clients to confidently navigate the intricate landscape of clinical data interpretation and regulatory compliance. We transcend in statistical and clinical programming, ensuring that complex clinical data is transformed into clear & concise submission packages and actionable insights.
3+
Number Of Ongoing Projects
4+
Number of Consulting Projects Supported
9+
Years of Average Staff Experience
12+
Global Studies Supported
Our Leaders Meet the visionary behind our success
Abdulkadir Lokhandvala
Founder
Abdul Lokhandvala is founding member of Altrid Analysis. He has over 14+ years of experience in drug development, with a specific focus on statistical programming. In addition to company's overall operational responsibilities, Abdul is directly involved in all statistical programming activities including automation and submission compliance review. Abdul is regular and long time volunteer of CDISC and he volunteers for PHUSE as well.
Core Value Driven by Integrity, Excellence and Cost Effectiveness
Integrity & Innovation
We operate with unwavering ethical standards while continuously pushing the boundaries of clinical data analysis. Our dual commitment means we deliver trustworthy results through innovative methodologies that transform complex datasets into valuable insights for decision-making.
Cost-effectiveness
Our streamlined processes and operational efficiency allow us to provide premium services at competitive rates. We optimize resource allocation across projects, ensuring you receive maximum value without compromising on quality or regulatory compliance.
Client Partnership
We function as an extension of your team rather than just a service provider. This collaborative approach includes transparent communication, shared problem-solving, and alignment with your strategic objectives to ensure our analytical deliverables advance your specific research goals.
Regulatory Adherence
Our comprehensive understanding of global regulatory requirements ensures your data submissions meet the required standards. We build compliance into every workflow, maintaining meticulous documentation that withstands regulatory scrutiny.
Technological Advancement
We continue to invest in tools and computing platform that enhance efficiency and achieve required level of automation. Our technical capabilities allow us to handle increasingly complex analysis while delivering deeper, more actionable findings.
Flexible Engagement
We adapt our service delivery models to accommodate your specific project needs and timelines. Whether you require comprehensive end-to-end data or targeted support, our scalable approach ensures you receive precisely the services you need.