Drug Development Journey
Drug Discovery & Pre Clinical
TAKE’s Role in Life Sciences
Clinical Trials PI-PIII
How CROs support Clinical Trials
OneClinical
How TAKE’s OneClinical Platform Improves Clinical Trials
pharmaREADY
How TAKE’s PharmaReady Suite Enables Regulatory Submissions
What Happens Once a Drug is Launched in the Market?
Post Marketing
What are Generics?
Generics
TAKE’s Unique, Proprietary Industry Networks
Industry Networks
TAKE’s Credentials
TAKE's Journey
Clinical Trials
Clinical Trials Services
To ensure successful outcomes for your clinical study, you require a partner who understands the objectives of the study,...
Clinical Data Services
Our Clinical Data Services (CDS) team delivers high-quality, timely and efficient services to meet all your clinical data services needs...
Clinical GCP Rapid Assessment
ICH GCP Addendum requires risk based, quality management of clinical trials; quality by design; effective CRO oversight;...
A Regulatory Outsourcing Partnership
A leading global biopharmaceutical company, headquartered in the USA, with a portfolio including medicines, vaccines,...
IDMP Imperative
To implement compliant and efficient processes, governance, and technology in line with IDMP Regulations...
Inspection Readiness
With increasing number of inspections worldwide, clinical functions are challenged to come up with scalable...
Oncology Phase 3 Rescue Trial
Given the complexity of clinical trials, despite best laid plans, certain trials can go off-track and this results,...
Regulatory Operations Smart Sourcing Strategy
The cost and complexity of meeting global regulatory requirements continue to increase...
Regulatory Services
Knowledge process outsourcing and technology capabilities to support our customers across...
RIM Maturity: A Strategic Path to RIM Excellence
Regulatory Information Management (RIM) is evolving as a Single Source of Truth for product data elements across the life sciences,...
The Case for ICH Compliance
The Clinical landscape has become increasingly challenging due to growing demand from regulators and the public...
Transformation to Risk Based Monitorin
Current processes in clinical operations generate high cost but often add little value...
Generics
Post Marketing
affiliateREADY
Affiliate Performance Insight & comparative performance and Proactive risk management,...
Digitally transformed pharmacovigilance
The necessity to change is fueled by regulatory agencies wanting to strive to better protect the patient,...
End-to-End Labeling
This End-to-End (E2E) Labeling project set out to provide the client with complete,...
Overhauling Pharmacovigilance processes
A mid-sized global pharmaceutical company, headquartered in Europe, required a program of work that would see three major projects,...
Oracle Argus on cloud based multi-tenant platform
Pharmacovigilance (PV) operations of mid-sized life sciences companies are facing challenges,...
Organizing your Global Labeling Function
Labeling is growing in importance. Regulators are increasingly emphasizing the need to deliver accurate,...
PV M&A Readiness & Integration
The TAKE Solutions Mergers & Acquisitions Readiness and Integration offering has been,...
Research Based Pharmaceutical Company
To achieve E2E visibility, TAKE Solutions worked with the client to ensure that there were effective linkages,...
Safety Medical Governance
Safety Medical Governance, which supports the safety monitoring of products and scientific processes within Pharmacovigilance,...
SafetyReady for Oracles Argus Safety Suite
We are domain experts in the areas of Clinical, Regulatory, Safety,...
Succeeding with Revised GVP Module IX
Signal management remains a cornerstone of ensuring patient safety. The release of the revised Good Pharmacovigilance Practices,...
Safety Medical Governance
Over the past decade, the nature of processes that pharmaceutical and biotech companies outsource has changed significantly...
Non Interventional Studies
Success in Non Interventional Studies largely depends on the ability to anticipate what can and cannot be performed in a routine setting,...
End-to-End (E2E) Labeling
Regulators are increasingly demanding greater visibility and oversight of the labeling process,...
End-To-End PV Optimization
Organic growth, mergers, acquisitions, and regulatory changes have resulted in an inefficient PV System -people,...
Nets
About labelnet
Established in 2011, labelnet provides an open yet confidential platform to network, share insights and experiences,...
About pvconnect
Established in 2006, pvconnect provides a neutral platform for PV leaders facing similar challenges to network,...
About pvnet
Established in 2001, pvnet provides a neutral platform for Pharmacovigilance (PV) leaders facing similar challenges,...
