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BizReport : White Papers : Biotechnology & Pharmaceuticals

Biotechnology & Pharmaceuticals

Are You Finding Signs Of Opioid Abuse In Your Health Data?

Learn how Artemis Health helped one employer find opioid abuse using their benefits data. >>

Are You Getting The Most Out of Your Pharmacy Benefits Data?

How the right information can help you manage your pharmacy costs and lead you to savings. >>

Find the Best 2018 Electronic Medical Records Software - Get FREE Customized Recommendations

Save time and money selecting the software system that is the best fit for your practice! >>

Stop Sacrificing Candidate Experience For Assessments

According to the Talent Board, 75% of employers are using some sort of pre-hire assessment. Traditional pre-hire assessments are scientific and predictive but provide a terrible experience for candidates. >>

The Gamification Playbook for Pharmaceutical Marketers

Find out how gamification can help pharma engage and motivate patients >>

Analysis with Concentric Market: Why Market Simulation is Unique

Simulation is a methodology that provides more actionable insights than any other tool. >>

Qualifying Clinical Site Personnel Using Embedded Automation

Four Guiding Rules for Embedding an eClinical Qualification Solution. >>

FDA Readiness Toolkit for Pharmaceutical Companies

Quality standards are defined by governing entities like the FDA in order to promote and sustain the quality of pharmaceutical products manufactured throughout the world. >>

5 Pharma Trends That Will Have the Biggest Impact in 2017

In this white paper, Patricia Santos-Serrao, RAC, MasterControl's director of clinical and regulatory solutions for pharmaceutical, blood, and biologics, discusses the five trends that will likely have the biggest impact on the pharmaceutical industry this year. >>

MasterControl Registrations for eCTD

Registering new products in different countries is a time-consuming and nerve-wracking process. >>

Ten Most Common Reasons for FDA 483 Inspectional Observations in Pharmaceutical Environments

This white paper outlines the most common reasons the FDA has issued This white paper outlines the most common reasons the FDA has issued Form 483 Inspectional Observations since the beginning of FY 2016 through the present date and shows how an Enterprise Quality Management System (EQMS) can help pharmaceutical companies avoid running afoul of the FDA and other like-minded regulatory bodies. >>

How 'Molecular Legos' Open Door to True Nanotechnology

By downloading this free guide, you agree to receive regular updates on the latest cool apps, product reviews, and giveaways from MakeUseOf. >>

How Nanotechnology is Changing the Future of Medicine

By downloading this free guide, you agree to receive regular updates on the latest cool apps, product reviews, and giveaways from MakeUseOf. >>

Biotech Breakthrough Opens Door to Designer Babies: Here's What You Need to Know

By downloading this free guide, you agree to receive regular updates on the latest cool apps, product reviews, and giveaways from MakeUseOf. >>

Brain Control With Light: It's Possible With Optogenetics

By downloading this free guide, you agree to receive regular updates on the latest cool apps, product reviews, and giveaways from MakeUseOf. >>

Providing Medical Affairs with Real Time Insights and Trends to Overcome Their 2016 Challenges

To reach potential, pharma must improve their use of medical insights, trends and analytics. >>

Pharmacists - Occupational Outlook

Pharmacists dispense prescription medications to patients and offer expertise in the safe use of prescriptions. >>

STAT - Special Report - Healthcare & Medical Content Roundup

Your daily dose of news in health and medicine focused specifically on the opioid crisis. >>

Morning Rounds - Healthcare & Medical Content Roundup

Your daily dose of news in health and medicine. >>

On Call - Healthcare & Medical Content Roundup

Your guide to the people and ideas shaping hospitals and transforming the delivery of health care. >>

The Readout - Healthcare & Medical Content Roundup

A guide to what's new in biotech. >>

Trump in 30 - Healthcare & Medical Content Roundup

The latest on what the Trump presidency means for health care, hospitals, drug companies, and medical research. >>

CAPA Toolkit

A CAPA program embodies the practices and processes that both FDA inspectors and ISO auditors consider singularly critical. >>

Clinical Study eTMF Manager

Go beyond document management! >>

ISO 13485 - Change? Do I Have to??

ISO has published the final draft of the latest ISO 13485 quality management standard for medical devices. >>

Proactive Compliance: Find The Right Prescription for Effective Life Science Data Governance

Learn to recognize data breach scenarios, automate compliance alerts and how to develop risk mitigation strategies. >>

Humanitarian Access to Unapproved Interventions in Public Health Emergencies of International Concern

Learn about humanitarian access in relation to public health emergencies. >>

Connecting the Dots: Health Information Technology Expansion and Health Disparities

Explore health IT expansion in this informative essay. >>

Strengthening the Detection of and Early Response to Public Health Emergencies

Learn lessons from the West Africa Ebola Epidemic. >>

Four Proposals to Help Improve the Medical Research Literature

Learn the problems with biomedical journals and proposals to improve them. >>

Paying Physicians to Presribe Generic Drugs and Follow-On Biologics in the United States

As spending on brand-name prescription medications continues to increase, find out the strategies to promote greater prescribing of generics. >>

A Road Map for Addressing Quality and Manufacturing Challenges in Life Sciences

Move beyond regulatory burdens to enable new collaborative models for growth with this eBook. >>

How Effective Training Management Can Help You Prevent Quality Issues

“Training is what helps turn the theory of quality into reality,” said Dave Hunter, product management director at MasterControl. Yet, for most companies in the regulated environment, quality is a concept manifested largely in paper instead of training through policies, SOPs, work instructions, manuals, and other materials. >>

Best Practice Guide for Implementing GLN in Trace, Chargeback & Rebate Processes

Reduce waste and increase accuracy in your healthcare incentive program. >>

How to Successfully Manage Your Suppliers and Ensure Product Safety and Compliance

Be vigilant about managing external parties to ensure compliance and product safety. >>

Risk Management: Best Practices for Medical Device Profitability

Success comes to those who consistently employ thorough analysis, collaborative business practices, and up-to-date technology. >>

ICH Q10 – Pharmaceutical Quality Systems - ‘An Opportunity for Us All'

If you have not yet reviewed the content of the ICH Q10 guideline and considered its impact on your company's quality system operations, then it makes good business sense for you to do so. >>

Six Corporate Oversights of Quality and Compliance Issues in Pharmaceutical Environments

This white paper presents six significant quality and compliance oversights that pharmaceutical companies may unknowingly propagate or encourage over time. >>

Engineering and Quality Teams in Medical Device Firms: Can We All Get Along?

A cross-functional team approach allows a medical device firm to bridge the gap between the product development and quality silos, with the ultimate goal of bringing new products to market faster, more efficiently and more economically. >>

Software Trends in the Medical Device Industry

Using software to help you improve efficiency and compliance while gaining a competitive edge. >>

The Challenges of Building an Effective Structure for Sponsor-CRO Partnership

The growth of Contract Research Organizations (CROs) as an industry is inevitable. When the global economy is thriving, life science companies are inclined to develop more products and hire CROs to complement in-house work. When the economy is in a slump as it is today, those companies still hire CROs, but for a different reason: to help cut overhead costs. >>

How Effective Document Management Helps Pharmaceutical Companies Accelerate Time to Market

This white paper will discuss common challenges pertaining to document control encountered by most drug companies from the preclinical stage through the post-market phase. >>

The Pharmaceutical Industry's Transition to Electronic Processes

To reduce inefficiency, FDA encourages pharmaceutical companies to automate processes. >>

How Software Helps Pharma/Biotech Maximize the Value of External Resources

For developed products, information on manufacturing batches, deviations, and CAPAs is imperative. Software that automates the production process and automatically generates these and other critical documents saves a tremendous amount of time and is impressive to potential investors. >>

How Software Helps Pharma/Biotech Maximize Value of External Resources

Perhaps more than any other industry, pharmaceutical and biotech companies rely on external resources--such as investors, strategic alliances, partnerships, licensing deals, and outside service providers--to finance products, expand geographically, lower costs, and, ultimately, increase revenues. >>

Complaint Handling as an Integral Part of FDA and ISO Compliance

This white paper prepared by MasterControl discusses the implications of consumer complaints in regulated environments and how companies can turn complaints into opportunities for improvement. >>

FDA Experts Offer Top Tips to Optimize Your eCTD Submission

For some companies accustomed to paper submissions, the new electronic format was a challenge. The eCTD format is a change for the better, however, because it's a more efficient way for the reviewers to evaluate the submissions. >>

ISO 17025: What it Means for You and Your Laboratory

For testing laboratories or laboratories that perform calibrations, certified compliance with ISO 17025 standards isn't always easy. While many labs effectively manage their business processes and compliance endeavors with manual or semi-manual processes, the proliferation of automation in life sciences and healthcare industries underscores the need for more streamlined and automated processes. >>

FDA Inspections of Clinical Investigators: Are You Ready?

In clinical research, there are two major regulatory concerns: patient safety and data integrity. >>

Managing Change Control to Comply with FDA and EU Regulations

Change is inevitable. That is why the concept of change control is critical, especially for pharmaceutical companies in FDA and EU-regulated environments, where inappropriate or “uncontrolled” changes could affect the safety of products and directly impact public health and safety. >>

Managing CLIA Compliance Costs: 6 Mistakes Every Laboratory Should Avoid

Clinical testing laboratories that perform testing in the United States must comply with Clinical Laboratory Improvement Act (CLIA) requirements. >>

How Quality and Compliance Can Help Reduce the Cost and Time Involved in Executing Clinical Trials

Quality, compliance, time, and cost are all critical concerns for life science companies conducting clinical trials. >>

Writing and Enforcing Your SOPs for GxP Compliance Success

The white paper summarizes the basic needs for SOPs and the subsequent benefits that SOPs provide. >>

BlogNotions Life Sciences Newsletter: Monthly eNewsletter Featuring Blogs from Industry Experts

Receive the BlogNotions monthly email series and stay up-to-date on the latest happenings in the life sciences space with insights and opinions from the web's most respected industry bloggers. >>

HIPAA and Beyond - How to Effectively Safeguard Electronic Protected Health Information

Explore how to go beyond HIPAA by learning how to use HIPAA as the starting point for your security program. >>

How Pharmaceutical CFOs are Turning a Top-line Problem into a Bottom-line Success in Today's Business Climate

In this white paper, learn how CFOs today are increasingly taking center stage in value creation. Also discover how CFOs are initiating and driving comprehensive Revenue Management projects to connect the disparate pieces of the revenue lifecycle in support of their new role as strategic business partners. >>

How R&D Lab Data Integration Drives Better, Faster Decisions

Improve the productivity of your analytical lab to make better R&D decisions, faster. >>

Building Novel Applications with Pipeline Pilot to Drive Next Generation Sequencing

This case study shows how scientists are streamlining the process of analyses of DNA sequence information. >>

Electronic Lab Notebooks in Drug Development

Learn how to implement and use an ELN in validated environments. >>

Transforming Materials Discovery with High-Throughput Computation

High-throughput quantum chemical calculations and virtual screening promise to revolutionize materials discovery. >>

Electronic Lab Notebook: Paperfree from Day One

ELN Drives Collaborative Research between Partners. >>

Speed Materials Innovation and Reduce R&D Costs with Scientific Information Management

Ideal for Executives and R&D Managers in the chemicals, materials or manufacturing industries to gain greater visibility into the R&D process to improve productivity, speed innovation and achieve top line growth. >>

Electronic Lab Notebook Speeds Drug Discovery

Find out how Millennium's ELN empowers chemists and biologists. >>

Quantifying the Value of Pipeline Pilot, the Accelrys Scientific Enterprise Platform

Learn the value of an enterprise R&D platform based on actual user experiences. >>

Accelrys Biological Registration: Mastering Biological R&D at Its Roots

In this IDC Health Insights white paper, learn how you can have the ability to effectively manage the large and complex research portfolios that are becoming increasingly difficult at large life science companies, a trend exacerbated by technology advances like high-throughput screening and further complicated by mergers and acquisitions. Ideal for Heads of Research IT and R&D Managers within Life Science companies. >>

Modeling & Simulation: The Return on Investment in Materials Science

Acquire an ROI of $3 to $9 for every $1 invested in scientific research. >>

Lower R&D IT Support Costs with Improved Scientific Data Integration and Management

A must-read for IT departments in today's science-driven industries whose R&D departments are looking to them to meet demanding innovation schedules. >>

Is a Hosted Electronic Lab Notebook Right for You?

Seven Ways to Assess if a Remotely Hosted ELN is Right for You. >>

IDC Manufacturing Insights: Accelerating Science-Led Innovation for Competitive Advantage

Learn why companies need to facilitate an enterprise approach to R&D informatics to manage all critical scientific data. >>

How Scientific Business Intelligence Can Drive Top Line Innovation Growth

Improve scientific data management across the global R&D enterprise to improve R&D productivity. Ideal for Scientists, R&D Managers and Executives in the scientific community. >>