The “Continuous Manufacturing Market (Small Molecules and Biologics), 2020 – 2030” report features an extensive study of the current market landscape and future opportunities for companies with capabilities in continuous manufacturing (both innovator companies with in-house expertise and contract manufacturers).
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Key Inclusions
§ A detailed assessment of the overall landscape
of companies with capabilities for continuous manufacturing, along with
information on a number of relevant parameters, such as year of establishment,
company size, purpose of manufacturing (in-house and contract services), scale
of operation (preclinical, clinical and commercial), location of headquarters,
location of manufacturing facilities, type of drug molecule (biologic and small
molecule), type of continuous manufacturing related service(s) offered (process
development, API manufacturing, intermediate manufacturing, drug product
manufacturing, and packaging and fill / finish), type of dosage form (solid and liquid), and
installed capacity and batch size (if available).
§
Elaborate profiles of some of the key contract
manufacturers active in the pharmaceutical and biopharmaceutical continuous
manufacturing market in North America, Europe and Asia-Pacific. Each profile
features an overview of the company, along with information related to its
service portfolio, continuous manufacturing capabilities and facilities, recent
developments and an informed future outlook.
§
An analysis of the various partnerships related to
continuous manufacturing, which have been established since 2013, based on
several parameters, such as year of an agreement, the type of partnership
(research agreements, facility development / establishment agreements,
technology enhancement agreements, service alliances, process development
agreements, manufacturing agreements and other relevant agreements), scale of
operation (preclinical, clinical and commercial), type of drug molecule
(biologic and small molecule), type of continuous manufacturing related service
(API manufacturing, intermediate manufacturing and end product manufacturing)
and type of dosage form (solid and liquid). It also provides the regional
distribution of the collaborations.
§
An analysis of the expansions related to continuous
manufacturing, which have been established since 2013, based on several
parameters, such as year of an expansion and the type of expansion (facility /
plant expansion, technology installation, technology enhancement and service
expansion), geographical location of the facility, scale of operation
(preclinical, clinical and commercial), type of drug molecule (biologic and
small molecule), type of continuous manufacturing related service (API
manufacturing, intermediate manufacturing and end product manufacturing) and
type of dosage form (solid and liquid).
§
An estimate of the global, continuous manufacturing
capacity, based on the capacities of various industry stakeholders (as
available on their respective company websites). The study examines the
distribution of capacity, based on the type of drug molecule (biologic and
small molecule), company size (small-sized, mid-sized and large), scale of
operation (preclinical, clinical and commercial), location of headquarters
(North America, Europe and Asia-Pacific) and location of manufacturing facilities (North America,
Europe and Asia-Pacific).
§
A study of the various grants that have been awarded to
research institutes engaged in projects related to continuous manufacturing,
between 2014 and 2019, highlighting multiple parameters, such as year of award,
type of grant, grant amount, focus area, support period, popular recipient
organizations, type of recipient organization, funding institute center,
funding mechanism and prominent program officers.
§
An in-depth analysis of the various patents that have been
filed / granted related to continuous manufacturing till 2019. It includes
information on key parameters, such as patent type, publication year,
geographical location, CPC symbol, emerging focus areas, type of applicant and
leading industry / non-industry players (in terms of the size of intellectual
property portfolio). It also features a three-dimensional bubble analysis
(based on patent citation count, publication year, extended geographical
reach), as well as a patent benchmarking and a detailed valuation analysis.
§
Initiatives taken by the leading pharmaceutical companies
(in terms of revenues), covering both partnered as well as in-house projects.
§
A review of the companies offering modular facilities /
modular cleanrooms, with information on their geographical location (North
America, Europe, Asia-Pacific and rest of the world), year of establishment,
company size (small-sized, mid-sized or large) and type of industries served
(pharmaceutical, biotechnology or others). It also includes information on the
recent projects undertaken / executed by the companies providing modular
facilities.
§
A case study of the companies offering technologies /
equipment (continuous blenders and mixers, continuous granulators, continuous
dryers, continuous compressors, continuous coaters, flow reactors, continuous
filtration, distillation and centrifugation equipment, continuous
chromatography, PAT technology and other technologies) that can potentially be
used in a continuous manufacturing process, providing information on the
geographical location of potential stakeholders and the type of technology /
equipment provided.
§
A case study on the roadmap for the adoption of continuous
manufacturing technique, discussing different strategies that can be followed
by the company in order to adopt this technology or transition from batch manufacturing
to continuous manufacturing.
The report also features the
likely distribution of the current and forecasted opportunity across important
market segments, mentioned below:
§
Purpose of
Manufacturing
§
In-House
§
Contract service
§
Scale of Operation
§
Commercial
§
Preclinical / Clinical
§
Type of Continuous
Manufacturing related Service
§
API Manufacturing
§
End Product
manufacturing
§
Type of Drug Molecule
§
Biologic
§
Small Molecule
§
Type of dosage form
§
Solid
§
Liquid
§
Key Geographical Regions
§
North America
§
Europe
§
Asia Pacific
§
Transcripts of
interviews held with the following senior level representatives of stakeholder
companies
§
Andrea Adamo, Founder and Chief Executive Officer, Zaiput
Flow technologies
§
Bayan Takizawa, Co-Founder and Chief Business Officer,
CONTINUUS Pharmaceuticals
§
Nick Thomson, Senior Director Chemical Research and
Development, Pfizer
§
Himanshu Gadgil, Director and Chief Scientific Officer,
Enzene Biosciences
§
Eric Fang, Chief Scientific Officer, Snapdragon Chemistry)
§
Ian Houson, Technical Project Manager, Continuous
Manufacturing and Crystallization, University of Strathclyde
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Key Questions
Answered
§
Who are the key players engaged in continuous manufacturing
of small molecules and biologics?
§ What
is the installed, global capacity for continuous manufacturing?
§ What
are the key growth drivers within this domain?
§ What
are the various paths to evolution within this industry?
§ Who
are the other key stakeholders (modular facility providers and technology /
equipment developers) in this domain?
§
How is the current and future market opportunity likely to
be distributed across key market segments?
You may also be interested in the following
titles:
1.
Pharmaceutical Contract Manufacturing
Market (2nd Edition), 2018-2028
2.
Biopharma Contract Manufacturing Market (3rd Edition), 2019 - 2030
3.
China Pharmaceutical Contract Manufacturing Services Market, 2020-2030
4.
China Biopharmaceutical Contract Manufacturing Market, 2020 - 2030
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