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Name *

Short description *

Year of foundation *

Address *

Latitude *

Longitude *

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Description of the plant

REGION * Select the region/continent where the facility is located.

Country in Europe Select the country where the facility is located.

Country in North America Select the country where the facility is located.

Country in APAC Select the country where the facility is located.

Country in MENAT

Country in LATAM

CATEGORY / PRODUCT Select the main category of the facility. If it covers more than one, create more plants.

Manufacturing stage / Product

Synthesis

Reactor scale for Chemical Synthesis

Purification Capabilities

Chemical Synthesis services

Biologics

ATMP

Cell therapy

Cell source

Tissue therapy

Gene Therapy Medicinal Products (GTMP)

Abs

ADC & NDC (Antibody / Nanobody - drug conjugate)

Complexity

Oligonucleotides

Vaccines

LBP Live Biotherapeutic Products

Platform

Bioreactor process

Bioreactor scale

Biologics services

Oligonucleotides

PARTICLE ENGINEERING

Milling

Granulation

Compaction

Extrusion

Blending

Drying

Sieving

Type of API Select the types of active ingredients you can work with in this facility.

Dosage forms Check the options closely and ensure you select all those dosage forms you are interested in manufacturing.

Injectables manufacturing process

Injectables primary packaging

Injectable formulations

Injectables special conditions

Small volume vials material

Small volume vials format

Large volume vials material

Large volume vials format

Glass ampoules

PFS (Prefilled Syringes)

Cartridges

Flexible bags / Infusion systems

Steriles manufacturing process

Sterile primary packaging

Bottles

Ophtalmic dispensers

Sterile form

Sterile semisolid forms

Oral solids / OSD

Tablets

Capsule size

Capsule load

Capsule closure

SoftGel capsules

Granules / Pellets form

Granules / Pellets formulation

Oral solids primary packaging

Oral liquid and semisolid forms

Oral liquids and semisolids primary packaging

Inhalation products

Aerosol

Powder

Nebulization

Topical, mucosal and transdermal products

Semisolid forms

Semisolid forms primary packaging

Liquid forms

Liquid forms primary packaging

Rectal and vaginal dosage forms

Formula

Skin products

Hair and scalp care products

Products for nails and cuticles

Oral hygiene products

Cosmetic form

Cosmetics services

Solid nutraceuticals

Tablets

Capsule size

Liquid and semisolid nutraceuticals

Nutraceuticals packaging

BATCH SIZE Provide the (qualitative) batch sizes that suit the facility. If desired, it can be detailed quantitatively in the “Description” section.

STAGE Select the stages (investigational/commercial) for which the facility is able or authorized to manufacture.

PHASE Select all clinical phases for which the facility could manufacture.

USE Select the uses (human/veterinary) for which the facility is able or authorized to manufacture.

THERAPEUTIC AREAS OF EXPERTISE (ATC) If applicable, select the therapeutic areas in which your production facility specializes (ATC classification). And in case of being restricted to these areas, please indicate it in the description.

OEB (Occupational Exposure Banding) Toxicity-related value. IMPORTANT: Select all those toxicities (according to the OEB classification) that you would be willing to work with, not just the maximum. Example: 3, 4 and 5.

BSL (Biological Safety Level) Biosafety-related value. IMPORTANT: Select all those biosafety levels (according to the BSL classification) that you would be willing to work with, not just the maximum. Example: 2 and 3.

CONTROLLED SUBSTANCES IMPORTANT: Please select all options that apply, not only the most restrictive one, as multiple selection is allowed.

CERTIFICATIONS Select those certifications you hold and those that you would be able and willing to obtain in the short term or with which you can easily comply.

ISO

IFS

MARKETS Select the markets for which you could manufacture.

SERVICES Carefully check all services and select only those you can perform. You can add those you perform through trusted partners ONLY if they do not require auditing and are not GMP activities.

Development services

Manufacturing

Analytical / QC services

Quality Assurance services

Regulatory services

Packaging

Logistics

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4 mL (2R)
5 mL (3R)
6 mL (4R)
10 mL (6R)
11.5 mL (8R)
13.5 mL (10R)
19 mL (15R)
26 mL (20R)
32.5 mL (25R)
37.5 mL (30R)
62 mL (50R)
123 mL (100R)
6.3 mL (5H)
8.3 mL (7H)
9.2 mL (8H)
14 mL (10H)
16 mL (15H)
24.9 mL (20H)
30.9 mL (25H)
36.6 mL (30H)
58.2 mL (50H)
116.2 mL (100H)
Other

ISO
World Health Organization (GMP / HACCP)
FDA (cGMP)
NSF
EMA (EU GMP)
PMDA/MHLW (Japan GMP)
NMPA (China GMP)
Health Canada (Canada GMP)
MHRA (UK GMP)
TGA (Australia GMP)
MFDS/KFDA (Republic of Korea GMP)
TITCK (Turkish Health Authorities)
UAE Ministry of Health & Prevention
SFDA (Saudi Food & Drug Authority)
ANMAT (Argentina nueva GMP)
ANVISA (Brazil B-GMP)
ISP (Chile BPM)
INVIMA
MSPAS
COFEPRIS
DIGEMID
Roszdravnadzor (Russia GMP)
IFS
SQF (Safe Quality Food)
BRCGS
Halal Research Council
ECOVADIS
French Service-Public (CIR)

FDA (USA)
EMA (EU)
PMDA (Japan)
NMPA (China)
MHRA (UK)
Health Canada (Canada)
TGA (Australia)
CDSCO (India)
MFDS (South Korea)
Turkish Health Authorities
EDE (UAE)
SFDA (Saudi Arabia)
ANMAT (Argentina)
ANVISA (Brazil)
ISP (Chile)
INVIMA (Colombia)
MSPAS (Guatemala)
COFEPRIS (Mexico)
DIGEMID (Peru)
Russian Health Authorities