Alimentiv Statistics specializes in Clinical Statistical Analysis, Clinical Trial Design and Data management of clinical research for pharmaceutical, biotechnology & medical device companies. Our unique expertise along with the flexibility and affordability of our services has helped make Alimentiv Statistics an integral and sought-after CRO.
Therapeutic Area agnostic statistical and data management expertise with over 40 years of providing quality expertise as a clinical trial CRO.
Operational excellence due to a team of eminently qualified and accredited statisticians resulting in over 95% of our clients being from satisfied referrals.
Our industry is one with high costs. Due to our niche focus, we are able to provide proposals that are highly competitive without compromising on outcome and quality.
The way your team plans, collects, manages, analyzes, interprets and prepares clinical data can significantly impact the success of your trial. Our statistical consultancy will help deliver objective perspective to clients.
Read MoreClients trust us to align study design and analyses with their business objectives and regulatory strategy by delivering a vital statistical strategy that helps mitigate risks during product development.
Read MoreWe provide dedicated clinical data management services from database build to database lock and archiving. Our team is committed to customizing data solutions that emphasize cost efficiency, data integrity and accuracy.
Read MoreIndustry research has shown that pharma and biotech companies are looking to avoid the trap of committing to inflexible contracts from a large contract or clinical research organizations. There is a real trend towards working with specialized CRO consulting firms like Alimentiv Statistics because of the unique expertise we can provide, the flexibility we can offer and the affordability of our services.
Access and download content such as whitepapers, reports, infographics, eGuides and articles on Biostatistics, Clinical Trial Design, Clinical Statistical Analysis, Data Management and the overall Clinical Trials Sector.
The way your team plans, collects, manages, controls, analyzes, interprets and prepares clinical data can significantly impact the success of your trial.
An insightful plan is the pathway to success. Alimentiv Statistics brings its over 35 years of experience to help solve the unique and complex challenges and requirements clients face throughout the clinical development process. Clients have trusted Alimentiv throughout the years to help align study design and analyses with their business objectives and regulatory strategy by delivering a vital statistical strategy that helps mitigate risks during product development.
Alimentiv Statistics’s advisory services help you conduct trials that are informative, compliant and cost-effective. Members of Alimentiv’s statistician team are accredited Professional Statisticians through both the Statistical Society of Canada (SSC) and the American Statistical Association (ASA) averaging over 15 years of progressive experience. Having such a breadth of experience among our statistical team enables us to provide our clients with services that make a real impact.
Our statisticians will provide guidance on your study design that will help answer your research questions with high confidence while meeting regulatory requirements and subject to business constraints.
Alimentiv has exceeded client expectations by providing timely, accurate data and analytics leading to expedited time-to-market and lower development costs.
Whether you call it clinical trial statistical analysis, Clinical Biostatistics, Biostatistics for clinical trials, Statistical analysis in clinical trials, or Statistical analysis for clinical trials, the way your team plans, collects manages controls, analyzes, interprets and prepares clinical data can significantly impact the success of your trial.
Alimentiv Statistics statistical or BioStatistics consulting services help you conduct trials that are informative, compliant and cost-effective. Clients trust us to align study design and analyses with their business objectives and regulatory strategy by delivering a vital statistical strategy that helps mitigate risks during product development.
Our statisticians can design your study to answer you research questions with high confidence while meeting regulatory requirements and subject to business constraints. During study implementation, ongoing analytical reporting supports centralized risk-based monitoring and safety review.
Members of Alimentiv’s statistician team are accredited Professional Statisticians through both the Statistical Society of Canada (SSC) and the American Statistical Association (ASA) averaging over 15 years of progressive experience. Having such a breadth of experience among our statistical team enables us to provide our clients with services that make a real impact.
Clinical data management (CDM) is an essential part in the data collection phase of clinical research. CDM ensures colelction, integration and availability of data, hopefully leading to high-quality, reliable, and statistically sound data is done in accordance with regulatory standards to obtain quality information that is complete and error-free.
The ultimate goal of CDM is to ensure that conclusions drawn from research are well supported by the data. Ultimately, Drug developers want ensure that the data delivered to regulatory bodies is reliable and that clinical data captured guides proper treatment decisions, which impact patient health.
Clinical data quality and integrity are key to clinical trial success. This helps ensure that drug companies deliver reliable data to regulatory bodies and helps guide proper treatment decisions for better patient health. McDougall Scientific provides dedicated clinical data management services from database build to database lock and archiving. Our method to capture, manage, clean and deliver data is efficient and scalable.
We offer a full suite of services utilizing traditional paper-based solutions and/or electronic data capture (EDC) solutions. Our team of clinical database programmers are well versed in a variety of leading EDC platforms. Our clinical data management team is committed to customizing data solutions that emphasize cost efficiency, data integrity and accuracy.
McDougall Scientific is a CDISC Platinum Solutions Provider, our team of Clinical Data Managers are certified by the Society for Clinical Data Management (SCDM) and are supported by compliance-driven Standard Operating Procedures. McDougall Scientific’s clinical data management services follow applicable laws and guidelines from regulatory agencies (e.g. ICH GCP and 21 CFR Part 11)
Consulting (strategic program planning, protocol review, etc.)
CRF/eCRF design and development
Real-time study metrics viewing and reporting
EDC consultation, design, selection
CRF Annotation & Review
Medical coding (MedDRA & WHODD)
Data capture and management using multiple EDC systems
Edit checks Programming & Testing
SAE Reconciliation
Paper setup and management
Query Management
Custom Programming
Data Management Plan (DMP)
Support for Safety Monitoring
Database build, design and implementation
SAE Reconciliation
Database lock
Data validation, review, cleaning, quality control
Database QA acceptance sampling prior to database lock
Database archival
Data processing through double data entry
Data captured using CDASH (Clinical Data Acquisition Standards Harmonization) standards.
Database transfer
24/7 access to secure real-time reports and metrics allows monitoring of site enrollment and activities
Follow benchmarks set by SCDM and CDISC
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