Medical White Papers

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Medical White Papers are in-depth articles aimed to educate and inform site visitors interested in medical research. Some of these papers are derived from sources where we have existing commercial relationships. Such articles are clearly labelled as sponsored content and are only accepted when the content is deemed to add value to the core editorial ethos of News Medical.

Breath Gas Analysis for COVID-19 Detection

Breath Gas Analysis for COVID-19 Detection

This article discusses the benefits for breath gas analysis and for COVID-19 detection applications.

From Ionicon Analytik Ges.m.b.H. 26 May 2020

The Role of HEK293 Cells in Gene Therapy

The Role of HEK293 Cells in Gene Therapy

This article details how gene therapy has been, and is still being, influenced by HEK293 cells.

From OXGENE 20 May 2020

Scalable Gene Therapy Manufacturing

Scalable Gene Therapy Manufacturing

This article discusses how OXGENE have produced a scalable gene therapy manufacturing process.

From OXGENE 20 May 2020

How Automation is Benefiting Gene Editing

How Automation is Benefiting Gene Editing

This article details how scientists and robots are working together to transform gene editing solutions.

From OXGENE 20 May 2020

A Guide to CRISPR Patent Rights

A Guide to CRISPR Patent Rights

This article details the history of CRISPR and the current patent rights for CRISPR treatment.

From OXGENE 20 May 2020

Future Applications of Gene Therapy for Heart Disease

Future Applications of Gene Therapy for Heart Disease

This article discusses the possible uses of gene therapy for a number of cardiovascular diseases and ailments.

From OXGENE 20 May 2020

The Importance of In Vivo Genome Editing Treatment

The Importance of In Vivo Genome Editing Treatment

This article discusses the world's first in vivo genome editing treatment, and how it could effect the future of medicine.

From OXGENE 20 May 2020

Developments of Quality Assured Automated CRISPR

Developments of Quality Assured Automated CRISPR

This article details the history of genome editing, and the resulting quality assured automated CRISPR today.

From OXGENE 20 May 2020

Pharmaceutical Development and Formulation Considerations

Pharmaceutical Development and Formulation Considerations

During expedited pharmaceutical development, a balance of formulation considerations must be made between reliability, yield and cost.

From DSI, a PLG Company 8 May 2020

Aligning Pharmaceutical Quality Systems and Product Development

Aligning Pharmaceutical Quality Systems and Product Development

Pharmaceutical quality system requirements must be considered during breakthrough product development with appropriate flexibility.

From DSI, a PLG Company 8 May 2020

Design and Implementation of Quality Pharmaceutical Systems

Design and Implementation of Quality Pharmaceutical Systems

Efficient design and implementation of quality pharmaceutical systems help to meet the expectations of investors, sponsors and regulators.

From DSI, a PLG Company 8 May 2020

Pharmaceutical Vendor Inspections, Audits and Qualification

Pharmaceutical Vendor Inspections, Audits and Qualification

Proactive routine evaluation of pharmaceutical vendors through inspections, audits and qualifications minimizes supply chain disruptions and quality issues.

From DSI, a PLG Company 8 May 2020

Management and Assessment of the Pharmaceutical Supply Chain

Management and Assessment of the Pharmaceutical Supply Chain

Needing capable development and oversight, the pharmaceutical supply chain is critical to supply goods to the market and the clinic.

From DSI, a PLG Company 8 May 2020

Chemistry, Manufacturing, and Controls Regulatory Affairs Support

Chemistry, Manufacturing, and Controls Regulatory Affairs Support

Chemistry, manufacturing and control information is collected during drug development and must be prepared to be submitted for regulatory affairs support.

From DSI, a PLG Company 8 May 2020

Identifying and Managing Pharma Contractors and Vendors

Identifying and Managing Pharma Contractors and Vendors

Identifying and managing reliable and technically competent pharma contractors and vendors is one of the best ways of minimizing drug development time.

From DSI, a PLG Company 8 May 2020

Optimizing and Validating Analytical Pharmaceutical Methods

Optimizing and Validating Analytical Pharmaceutical Methods

Spanning the methodological lifecycle, DSI can help with optimizing and validating analytical pharmaceutical methods from creation to implementation.

From DSI, a PLG Company 8 May 2020

Pharmaceutical Regulatory Submission Preparation and Management

Pharmaceutical Regulatory Submission Preparation and Management

Required by a regulatory agency, pharmaceutical regulatory submissions are information packets to determine whether clinical trials can proceed.

From DSI, a PLG Company 8 May 2020

Meeting Pharmaceutical Regulatory Challenges

Meeting Pharmaceutical Regulatory Challenges

Often pharmaceutical regulatory submissions meet challenges, including requests for additional data, clarification, reanalysis and other issues to be addressed.

From DSI, a PLG Company 8 May 2020

How LIMS Can Solve Biobanking Informatics Challenges

How LIMS Can Solve Biobanking Informatics Challenges

This article discusses how COTS LIMS can be used to solve the challenges associated with biobanking informatics.

From LabVantage Solutions 16 Apr 2020

How LIMS Can Be Used to Improve Biobanking

How LIMS Can Be Used to Improve Biobanking

This article discusses how LIMS can be used to improve biobanking for the pharmaceutical industry.

From LabVantage Solutions 16 Apr 2020

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