Haleus provides quality medical writing from IND application to post-marketing writing across a broad range of therapeutic areas..
We have an organized Data Review Committee; an independent non-biased panel and taking care of patient safety through periodic review of the clinical study data.
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We provide end to end bio-statistic service starting from Planning, execution, reporting and submission as per the study needs.
Thorough site management is a crucial factor in clinical trials. Haleus provides professional services and assistance to the site (investigators and other staff).
Project management is essential to fulfil the study and regulatory requirements within the timeframe.
Clinical monitoring is a key for the successful conduct of the clinical study in compliance with the protocol, ICH GCP, and applicable regulatory guideline(s).
Maintaining quality compliance throughout the study is key of authenticate clinical study data, specifically in the complex study design.
Our Bioanalytical Experts have hands-on experience in managing complex molecules analysis using robust LCMS/MS Methods.
We have efficient collaborations with NABL accredited laboratories in the India which have long term and short-term sample storage facility as well.
Management of the safety data and adverse events in a clinical trial is significant throughout the clinical conduct of the study.
Haleus provides quality medical writing from IND application to post-marketing writing across a broad range of therapeutic areas
Haleus provides full regulatory services starting from the initial regulatory submission to marketing approval of the drug.
Pre-clinical study plays a key role in drug development and marketing approval.
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HaleUS
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