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Our Services



DevOps

Why Does DevOps Matter ?


The IT industry, banking systems, shopping and entertainment, have been changed by internet and applications. The software has now become an integral part of every business. Interaction with customers has now been made easier by online applications and online services on every possible device. Logistics, communication and operations are part of the value chain that has been transformed by software. Using industrial automation, companies have transformed how they build and design their software same way as they transformed how they build, design and deliver their physical goods.





Cloud Transformation

Why Perform a Cloud Transformation ?


Business Benefits

Gain a competitive advantage and enjoy up to 53% faster revenue.
Gain more agility with up to 21% faster time to market.
Innovate more quickly to stay on the cutting edge of your niche.

Development Benefits

Spend less time maintaining build servers.
Benefit from automated software updates.
Utilize the latest cloud technology and stay up-to-date.
Reduce administration burdens.

User Benefits

Easily implement remote work opportunities for developers.
Achieve easier collaboration and receive up to a 400% return on investment.
Gain easier access to information.





Healthcare


Statistical Programming


Our Statistical Programming team provide full service for all phases of clinical trials end to end for BLA, NDA and ANDA submission, including but not limited to Study Design, Clinical Programming and Validation for Standard(SDTM) and Analysis (ADaM) Data Model, Analysis and Reporting.

>>   Clinical Trial Design
>>   Developing protocols
>>   Developing Statistical Analysis Plan (SAP)
>>   SDTM, ADaM Programming and Validation
>>   Tables, Listing and Figures(TLF?S) Programming and Validation
>>   Independent Data Monitoring Committees (IDMCs)
>>   Interim and Final Analysis
>>   Submissions of ISS/ISE and CSRs
>>   Study Data Reviewer?s Guide (SDRG)
>>   Analysis Data Reviewer?s Guide (ADRG)
>>   Define.xml

Clinical Data Management


We provides full range of clinical data management services for local, and global clinical research studies. We are handling all phases of clinical trials(Phase-I to Phase-IV) across all the therapy areas. We are developing customized Clinical Data Management activities based on client needs from from early study setup to closeout(Case Report form(eCRF) design and annotation, Database Design, Query Management, UAT Testing, Medical coding, DB-lock activities) as per Regulatory Guidelines.

Regulatory Guidelines we follow:

>>   E6(R2) Good Clinical Practice(ICH GCP-E6)
>>   Code of Federal Regulations (CFR), 21 CFR Part 11
>>   Clinical Data Interchange Standards Consortium(CDISC)
>>   Good Clinical Data Management Practices (GCDMP)
>>   Clinical Data Acquisition Standards Harmonization (CDASH)

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