Your partner in transforming the industry
Avenga is a technology partner to the leading pharmaceutical, biotech and medical firms, contract research organizations (CROs), clinical research institutions, and pharmacovigilance vendors in transforming the future of the pharmaceutical industry.
Pharma & life sciences industry facts
7.5
years is the average length for the clinical trial research phase.
Source: Chi-Jen Lee, Clinical Trials of Drugs and Biopharmaceuticals
80%
of clinical trials do not manage to recruit and retain enough patients and fail to meet enrollment timelines.
Source: Clinical trial delays: America’s patient recruitment dilemma
$2.6 bn
is the total cost of developing one new drug and making it through the FDA approval phase.
Source: Duggan & Pence, Approval Rate for Drugs Entering Clinical Development, 2019
Our Pharma & Life Sciences Expertise
Custom software development for preclinical & clinical trials, drug commercialization, manufacturing, distribution, and safety.
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Preclinical/ Clinical Trial Management Software Development
Accelerate your commercial drug development and regulatory processes with a secure and complaint preclinical & clinical trial management software, such as:
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- ePRO (Electronic Patient-Reported Outcome) data collection
- eDC (Electronic Data Capture) software development
- eCTMS (Clinical Trial Management System) development
- eCRF (Electronic Case Report Forms) integration
- eCOA (Electronic Clinical Outcome Assessment) integration
- Patient recruitment solutions
- Early clinical data management solutions
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Pharma Manufacturing and Commercialization Software Development
Stay organized, maintain strict quality management and streamline pharma manufacturing to meet client’s specifications and regulatory requirements with the help of:
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- ERP (Enterprise Resource Planning) software
- MES (Manufacturing Execution Systems)
- MOM (Manufacturing Operations Management) platforms
- MRP (Material Requirements Planning) platforms
- Production planning and procurement software
- Traceability and recall management software
- Product quality management software
- PA (Prior Authorisation) solutions
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Pharma Distribution Software Development
Streamline the flow of ordering, selling, warehousing and shipping pharmaceutical and life sciences products with the help of:
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- Accounting, customer, and service management
- Automation and inventory software
- Warehouse management solutions
- Logistics solutions
- Supply chain management software
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Drug Safety Software Development
Build pharmacovigilance software or drug safety solutions that lower your operational costs and are fully compliant with pharmaceutical regulations with the help of:
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- Adverse drug reaction reporting applications
- Adverse events database development
- Integration of workflows and gateways with the WHO drug dictionary
- Medical request information management software
- Drug safety monitoring software
All You Need to Know About Digital Clinical Trial Management in the 2020s
We created for you a 25-pager whitepaper discussing the most important new technologies that are transforming the clinical trial processes. Explore how digital tools for clinical trial management can help you to bring treatment to patients faster and with a lower cost.
What we do
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Do you need to speed up drug development cycles, introduce real-time insights on sales and user data, enhance operational efficiency, engage customers, improve control and security compliance, and deliver first-rate patient outcomes?
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We, at Avenga, deliver full-spectrum services to Life Science and Pharma enterprises globally and make innovation happen. We help our clients drive digital transformation to face tomorrow’s challenges in introducing new drugs, and to cure what is not curable today.
Pharma technology solutions
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Data Science
- Adaptive clinical trials
- Analytics and reporting, with adaptability
- Digital transformation through doctor-patient connection, iOT, and wearables
- Getting access to the best doctors
- Holistic and consolidated approach to data management
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Clinical Trial Management solutions
- Drug development platforms
- Drug simulation software
- Trial’s management and reporting
- Patient recruitment systems
- ECM software
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Pharmacovigilance
- Incident reporting
- AI & ML solutions for pharmacovigilance (chatbots, etc.)
- Pharmacovigilance IT architecture
- Signal detection software
- Adverse event processing
- Pharmacovigilance assessment
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Pharma Sales & Marketing
- Sales, prescriber and claims data management
- CRM and Salesforce automation solutions
- Closed Loop marketing
- KOL management
- Conversational AI & NLP chatbots
- Assisting sales with leads using a business network
- Working with pre-sales to qualify opportunities and identify gaps
- Assist in recruiting partners
- Training
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Data Management
- Electronic Data Capture systems (eDC)
- Electronic patient reporting outcomes (ePRO)
- Secure data storage for your digital assets
- Governance software
- Phenotyping data capture
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Precision Medicine for Clinical Trials
- Web and cloud solutions for precision medicine for pharma
- Companion diagnostic (CDx) tests development
- Biomarker analysis
- Genomic data integration and data processing
- Molecular workflows management
How technology transforms pharma
2x
more clinical trials using biomarkers are likely to get approved.
Source: Wong, C., Estimation of clinical trial success rates, 2018
42%
of novel molecular treatments that were approved by the FDA in 2018 were precision medicines.
Source: FDA, New Drug Therapy Approvals, 2019
6/10
tech giants are diversifying in pharma and healthcare.
Source: Deloitte, Global Life Sciences Outlook, 2019
Avenga achieved ISO/IEC 27001:2013 certification for the information security management system (ISMS).
ISO/IEC 27001:2013 certification is a set of best practices and controls regarding cybersecurity risks. It emphasizes data confidentiality, integrity, and availability and is widely recognized as the gold standard for ISMS.
Case studies
See how we reshaped the business of global Pharma and Life Science providers by helping them to deliver improved patient outcomes through digital services.
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Telehealth suite for an improved patient experience
M3 Health | Pharma & Life SciencesLearn moreA set of mature telehealth applications integrated in the health cost containment and care management platform.
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Innovative Drug Ordering System for Life Sciences
QPharma | Pharma & Life SciencesLearn moreGroup millions of patients globally to negotiate the lowest drug prices possible.
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Predictive Solution for Enhanced Clinical Trial Management
CRO for pharma and biotech companies | Pharma & Life SciencesLearn moreAccess terabytes of well-structured data on clinical trials in real-time.
Technology Capabilities for Pharma & Life Sciences
We help pharma & life sciences organizations develop software for the entire pharmaceutical lifecycle, starting from the component research to drug approval. Our goal is to help our clients optimize their current business processes and bring drugs to market faster.
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Mobile enablement and connectivity
- Native, web, hybrid clinician app development for Android and iOS
- Wireless enablement using Bluetooth and BLE
- Secure mobile architecture development
- Machine to machine mobile solutions
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Software testing and quality engineering services
- Intelligent test automation
- Iterative testing
- Cross-platform app testing
- Performance and network testing
- Security QA
- Pattern mining and QA analytics
Avenga’s subject-matter experts (SMEs) and technical professionals are ready to help and find solutions for your struggles.
What clients have to say
Why Avenga?
4300+
professionals
410+
happy clients
20+
years of experience
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We have the experience.
Avenga has a proven track record of delivering excellence for life sciences, pharma, biotech and CRO’s (Contract Research Organizations). For over 15 years, we have maintained and grown ongoing long-term collaborations with the world’s leading pharma & life sciences companies. At Avenga, we combine innovations and technology to tailor and support IT solutions for drug product related operations including clinical trials management, pharma sales enablement, patient engagement portals, industry-specific education, e-prescriptions, integrations with EMR and PMS, legacy systems migration, and a lot more.
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We help you outpace the competition.
Avenga helps you anticipate the trends in biotech & pharma to increase your delivery speed and outcomes. We have the expertise in advanced software development solutions and can fill in your technology gaps with the right people with the right knowledge. We help enterprises redefine the patient experience and incorporate our expertise for life sciences and pharma into a pragmatic value delivery.
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We know the regulations and adhere to them.
Avenga stays abreast of the latest regulations and policies in the pharma and life sciences sector, like FDA, HIPAA, HINTECH, and GDPR. Unlike other product development firms, Avenga software development services are tailored to the highly regulated pharmaceutical & life sciences industry. We understand the complexity of the present-day challenges faced by biotech firms and CROs and implement innovative tech solutions to address these challenges. We meticulously adhere to the strictest Standard Operating Procedures (SOPs) that concern clinical data management and monitoring across all our development stages.
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We have the right people in the right place.
More than 4,300 Avenga professionals across 31 offices are working hard to deliver exceptional impact for our customers and help pharma and life sciences bring discoveries to life. We are proud to have a vast number of software development experts that have already built flexible, compliant and progressive solutions for top pharmaceutical and life sciences companies in the world.
