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We all know the fact that Malaysia is one of the most flexible developing nations globally. They are advancing with the greatest growth in the economic and other marketing fields.

It features an in-depth analysis, highlighting the various types of elastomeric closures including stoppers.

An in-depth analysis of peptide platform and library service providers, featuring information on their company details

Around USD 3 billion was raised through secondary offerings, representing more than 50% of the total capital raised by industry players till July 2019.

Majority of the industry players (70%) are very large firms (having more than 500 employees). North America is the current hub

A detailed assessment of the current market landscape of drug developers engaged in the development of TIL-based therapies

A discussion on key technological innovations (tools / technologies), such as advanced grippers, artificial intelligence

Given their flexibility and price to functionality ratio, cobots represent an ideal entry-level, automation model for both small and established companies

The report features an extensive study of the current market landscape and future opportunities associated with proteome profiling service providers

An in-depth analysis of more than 260 cell therapy developers that are anticipated to partner with cell and gene therapy

A competitiveness analysis of pharmaceutical vial manufacturers, segmented into four categories, namely small, mid-sized companies, and large and very large companies

An analysis of the partnerships and expansions that have been established in this domain, in the recent past.

An insightful geographical benchmarking of the capabilities of companies of various sizes, highlighting the key focus areas

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A comparative analysis of the needs of different stakeholders (drug developers, diagnostic developers

Several companies have already developed / are developing analytical tests for novel cancer biomarkers (TMB, MSI / MMR and TILs), intended to assist physicians in making personalized treatment decisions.

The projected future opportunity is expected to be distributed across different application areas, types of analytical techniques used and various global regions

A discussion on various steps involved in development operations of companion diagnostics

An analysis of the big biopharma players engaged in this domain, featuring a heat map based on various parameters

Several pipeline candidates have recently entered mid to late-stage (phase II and above) trials and are anticipated to enter the market over the next 5-10 years.

The pipeline features drug candidates that target a wide range of biological antigens based on different antibody formats through novel mechanisms of action; more than 50% of these act by retargeting or activation of T-Cells

An analysis of the initiatives of big biopharma players engaged in this domain.

An analysis of the various partnerships pertaining to non-invasive cancer diagnostics

The financial opportunity within the liquid biopsy and other non-invasive cancer diagnostics market has been analyzed across

Presently, nearly 300 non-invasive diagnostic tests, designed for the detection of various types of cancers, are either already available in the market or under development across the world

An analysis of the various partnerships pertaining to non-invasive cancer diagnostics, which have been established between 2016 and 2019.

A detailed discussion on the cost implications across various steps of the HFE and usability testing process.

Human factors engineering and usability testing have now become an essential part of product design across almost all industries

Players involved in this domain are steadily expanding their capabilities in order to enhance their respective service portfolios and gain an advantage over competitor firms

Based on the revenues generated from different services for usability testing, currently, the maximum share is expected to be generated through evaluative testing methodologies (61%), followed by generative testing methodologies (39%).

A case study comparing the key characteristics of large molecule and small molecule drugs, along with details on the various steps involved in their respective manufacturing processes

In order to meet the growing demand for their services, Chinese CMOs are actively consolidating / expanding their capabilities through partnerships and / or dedicated expansion initiatives

Big pharma players have also made significant investments in this region, including establishing new facilities, expanding existing R&D centers and growing manufacturing facilities, focused on biotherapeutics

An analysis of the initiatives of big biopharma players engaged in this domain.

A discussion on the upcoming opportunities (such as development of companion diagnostics, emerging technologies for biomarker assessment, and others) that are likely to impact the evolution of this market over the coming years

Several companies have already developed / are developing analytical tests for novel cancer biomarkers (TMB, MSI / MMR and TILs), intended to assist physicians in making personalized treatment decisions.

Several novel biomarkers are presently under investigation for a variety of cancer indications; the initiatives of big pharmaceutical companies are indicative of the growing interest in this domain

A detailed analysis of ongoing, biomarker-based clinical trials initiated by big pharmaceutical companies.

An analysis of the investments made, including seed financing, venture capital financing

Several therapy candidates are being investigated both as monotherapies and in combination

Presently, over 150 neoantigen targeted therapies are being evaluated for advanced cancer indications and are designed for delivery via different routes of administration

An in-depth analysis of the various patents that have been filed / granted related to neoantigens.

n fact, more than 6,000 patents were filed / granted related to neoantigen targeted therapies, since 1978.

 A survey analysis featuring inputs solicited from various experts who are directly / indirectly involved in providing regulatory affairs management services to medical device developers