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Key Inclusions
§
A detailed review of
the overall landscape of companies offering contract services for the manufacturing
of HPAPIs and cytotoxic drugs, along with information on year of establishment,
company size, scale of operation (preclinical, clinical and commercial),
location of headquarters, number and location of manufacturing facilities,
facility size, type of service(s) offered (clinical manufacturing, commercial
manufacturing, analytical testing, scale-up, process development /
pre-formulation, formulation development, stability studies, regulatory support
and fill / finish and packaging), type of product manufactured (HPAPIs and
highly potent finished dosage forms), type of pharmacological molecule (biologics
and small molecules), type of highly potent finished dosage form manufactured
(capsules, granules, injectables, liquids and tablets), and type of primary
packaging used (ampoules, blisters, prefilled syringes, conventional syringes,
vials and others).
§
A competitiveness
analysis of HPAPI and cytotoxic drugs contract manufacturers, taking into
consideration supplier strength (based on company size and its experience in
this field) and service strength (based on scale of operation, type of
service(s) offered, type of product(s) manufactured, number and location of
manufacturing facilities, type of highly potent finished dosage forms
manufactured and type of primary packaging used).
§
Elaborate profiles of
the key players (shortlisted based on a proprietary criterion) that offer a
diverse range of capabilities for the development, manufacturing and packaging
of HPAPIs and cytotoxic drugs, across North America, Europe and Asia Pacific.
Each profile includes a brief overview of the company, its year of establishment,
location of headquarters, number of employees and financial information (if
available). In addition to this, the profile includes information on the various
HPAPIs / cytotoxic dugs manufacturing services offered by the company, along
with the location of their manufacturing facilities. Further, we have provided
the recent developments of the company and an informed future outlook.
§
An analysis of the various
partnerships pertaining to the contract manufacturing of HPAPIs and cytotoxic
drugs, which have been established since 2014, based on several parameters,
such as the year of partnership, type of partnership, type of product, scale of
operation, company size, amount invested in acquisitions, most active player and geographical analysis.
§ An analysis of the various expansion
initiatives undertaken by service providers, in order to augment their
respective HPAPI and cytotoxic drug manufacturing capabilities, over the period
2014-2019, taking into consideration several relevant parameters, such as year
of expansion, type of expansion (capacity expansion, facility expansion and new
facility), scale of operation (preclinical, clinical and commercial), type of
product manufactured (HPAPIs and highly potent finished dosage forms), and
location of manufacturing facility.
§ An estimate of the overall, installed capacity
for manufacturing HPAPIs and cytotoxic drugs based on data reported by industry
stakeholders in the public domain; it highlights the distribution of available
HPAPIs and cytotoxic drugs production capacity on the basis of company size
(small-sized, mid-sized, large and very large companies), scale of operation
(preclinical, clinical and commercial), and across key geographical regions
(North America, Europe, Asia Pacific and rest of the world).
§ A qualitative analysis, highlighting the
various factors that need to be taken into consideration by highly potent drug
developers while deciding whether to manufacture their respective products
in-house or engage the services of a CMO.
§ A discussion on affiliated trends, key drivers
and challenges which are likely to impact the industry’s evolution, under a
comprehensive SWOT framework; it includes a Harvey ball analysis, highlighting
the relative effect of each SWOT parameter on the overall industry.
§ A case study on the antibody drug conjugates
(ADCs) manufacturing market, highlighting a list of contract service providers
and in-house manufacturers that are currently active in this space.
Additionally, it includes a detailed set of analyses of these companies based
on several parameters, such as year of establishment, company size, scale of
operation (preclinical, clinical and commercial), location of headquarters,
number and location of manufacturing facilities, and type of service(s)
offered.
The report also features the likely
distribution of the current and forecasted opportunity across important market
segments, mentioned below:
§ Type
of Product
§ HPAPIs
§ Highly
Potent Finished Dosage Forms
§
Company Size
§
Small-sized
§
Mid-sized
§
Large / Very Large
§ Scale
of Operation
§
Preclinical / Clinical
§
Commercial
§ Type
of Pharmacological Molecule
§
Small Molecules
§
Biologics
§ Type
of Highly Potent Finished Dosage Form
§ Injectables
§ Oral
Solids
§ Creams
§ Others
§ Key
geographical regions
§ North
America
§ Europe
§ Asia
Pacific
§ Rest
of the World
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Key Questions Answered
§
Who are the key manufacturers of HPAPIs and cytotoxic
drugs, across the world?
§
What kind of partnership models are commonly adopted by
stakeholders in this domain?
§
What is the current, installed contract manufacturing
capacity for HPAPIs?
§
What are the key factors influencing the make
(manufacture in-house) versus buy (outsource) decision related to HPAPIs
and cytotoxic drugs?
§ What
are the key drivers and growth constraints in HPAPI and cytotoxic drugs
manufacturing market?
§
How is the current and future market opportunity likely to
be distributed across key market segments?
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Contact Us
Gaurav Chaudhary
+1 (415) 800 3415
gaurav.chaudhary@rootsanalysis.com