🇵🇱 PAŃSTWOWY INSTYTUT WETERYNARYJNY PL
Materials & polymersConstructionMicrobiologyFood & beveragesWater & wastewater
PAŃSTWOWY INSTYTUT WETERYNARYJNY is a laboratory accredited by PCA under number AB 1090 (Puławy, Poland). Its accreditation scope covers 29 test methods in the following areas: Materials & polymers, Construction, Microbiology, Food & beverages. Test objects include: Biological material of fish origin, Biological material from salmonid fish, Biological material from crustaceans, Serum of solipeds. Most frequently used techniques: Stage 1: method of virus propagation and isolation in continuous ce…, RT-PCR method, Culture method with biochemical and microscopic confirmation.
At a glance
- Accreditation number: PCA AB 1090
- Methods in scope: 29
- Types of test objects: 18
- Techniques used: 20
- City: Puławy, Poland
- Accreditation number
- AB 1090
- Accreditation body
- PCA
- Address
- - PAŃSTWOWY INSTYTUT BADAWCZY, Al. Partyzantów 57, 24-100-Puławy, Dział Parazytologii i Chorób Inwazyjnych, Chorób Pszczół i Chorób Zwierząt
- City
- Puławy, Poland
What this laboratory tests (18)
- Biological material of fish origin — 8 methods
- Biological material from salmonid fish — 3 methods
- Biological material from crustaceans — 2 methods
- Serum of solipeds — 2 methods
- Animal serum — 1 method
- Bee brood — 1 method
- Bee brood, bees, honey (sugar food stores), beeswax — 1 method
- Bees — 1 method
- Biological material originating from molluscs — 1 method
- Bovine brain stem — 1 method
- Brain stem of cattle, sheep and goats — 1 method
- Consumer products intended for humans including food / fish meat — 1 method
- Intestines of carnivorous animals — 1 method
- Meat samples from animal species susceptible to Trichinella infestation — 1 method
- Organic fertilizers — 1 method
- and 3 more
Analytical techniques used (20)
- Stage 1: method of virus propagation and isolation in continuous cell lines; Stage 2: ELISA method — 4 methods
- RT-PCR method — 3 methods
- Culture method with biochemical and microscopic confirmation — 2 methods
- IFAT method — 2 methods
- Method of isolation, incubation and microscopic observation — 2 methods
- Real Time PCR method — 2 methods
- Bulk sample leaching using magnetic stirring; Reference method — 1 method
- Culture method with microscopic confirmation — 1 method
- Etching method — 1 method
- Filtration, immunomagnetic separation and direct immunofluorescence method — 1 method
- Histological method — 1 method
- Immunohistochemical method — 1 method
- Macroscopic method — 1 method
- Microscopic method — 1 method
- Nested PCR method — 1 method
- and 5 more
Laboratory sections (2)
- Department of Parasitology and Invasive Diseases, Bee Diseases and Aquatic Animal Diseases — 27 methods
- Scientific Support of Research Potential Department — 2 methods
Laboratory locations
- PAŃSTWOWY INSTYTUT WETERYNARYJNY (main site) — Al. Partyzantów 57, 24-100 Puławy
- Department of Parasitology and Invasive Diseases, Bee Diseases and Aquatic Animal Diseases — Al. Partyzantów 57, 24-100 Puławy
- Scientific Support of Research Potential Department — Al. Partyzantów 57, 24-100 Puławy
Certificate information
- Issue date
- 27.07.2026
- Issue no.
- 22
Accreditation scope — test methods (29)
| No. | Test object | Methodology / Parameters | Technique | Reference document | |
|---|---|---|---|---|---|
| Scientific Support of Research Potential Department | |||||
| 1 | Brain stem of cattle, sheep and goats | Presence of morphological changes specific for bovine spongiform encephalopathy and scrapie in sheep and goats | Histological method | DNW/PB-01 issue 4 of 2026-03-11 | |
| 2 | Bovine brain stem | Presence of the prion protein specific for bovine spongiform encephalopathy. | Immunohistochemical method | DNW/PB-02 issue 4 of 2026-03-11 | |
| Department of Parasitology and Invasive Diseases, Bee Diseases and Aquatic Animal Diseases | |||||
| 3 | Biological material of fish origin | Presence of VHS virus | Stage 1: method of virus propagation and isolation in continuous cell lines; Stage 2: ELISA method | DPI/PB-52 issue 2 of 2026-01-16 | |
| 4 | Biological material from salmonid fish | Presence of IHN virus | Stage 1: method of virus propagation and isolation in continuous cell lines; Stage 2: ELISA method | DPI/PB-53 issue 2 of 2026-01-16 | |
| 5 | Biological material from salmonid fish | Presence of IPN virus | Stage 1: method of virus propagation and isolation in continuous cell lines; Stage 2: ELISA method | DPI/PB-54 issue 2 of 2026-01-16 | |
| 6 | Biological material from salmonid fish | Presence of the HPR0 variant of ISA virus / Presence of the HPR-deleted variant of ISA virus | RT-PCR method | DPI/PB-60 issue 2 of 2026-01-16 | |
| 7 | Biological material of fish origin | Presence of bacteria | Culture method with biochemical and microscopic confirmation | DPI/PB-55 issue 2 of 2026-01-16 | |
| 8 | Biological material of fish origin | Presence of EHN virus genetic material | Stage 1: method of virus propagation and isolation in continuous cell lines; Stage 2: PCR/RFLP method | DPI/PB-61 issue 2 of 2026-01-16 | |
| 9 | Biological material of fish origin | Presence of SVC virus | Stage 1: method of virus propagation and isolation in continuous cell lines; Stage 2: ELISA method | DPI/PB-56 issue 2 of 2026-01-16 | |
| 10 | Biological material originating from molluscs | Presence of Marteilia sp. and Bonamia sp. | Microscopic method | DPI/PB-57 issue 2 of 2026-01-16 | |
| 11 | Biological material of fish origin | Presence of virus genetic material: VHS, IHN, IPN, SVC and SAV | RT-PCR method | DPI/PB-62 issue 2 of 2026-01-16 | |
| 12 | Biological material of fish origin | Presence of KHV virus genetic material | Real Time PCR method | DPI/PB-63 issue 2 of 2026-01-16 | |
| 13 | Biological material from crustaceans | Presence of virus genetic material: WSSV | Nested PCR method | DPI/PB-64 issue 2 of 2026-01-16 | |
| 14 | Biological material from crustaceans | Presence of virus genetic material: YHV, TSV | RT-PCR method | DPI/PB-64 issue 2 of 2026-01-16 | |
| 15 | Biological material of fish origin | Presence of virus genetic material: VHS, IHN, ISA | Real-Time RT-PCR method | DPI/PB-65 issue 2 of 2026-01-16 | |
| 16 | Biological material of fish origin | Presence of Renibacterium salmoninarum genetic material | Real Time PCR method | DPI/PB-66 issue 2 of 2026-01-16 | |
| 17 | Serum of solipeds | Presence of antibodies to Trypanosoma equiperdum | OWD method | DPI/PB-09 issue 3 of 2026-04-21 | |
| 18 | Serum of solipeds | Presence of antibodies to Trypanosoma equiperdum | IFAT method | DPI/PB-12 issue 2 of 2026-01-16 | |
| 19 | Animal serum | Presence of antibodies to Toxoplasma gondii | IFAT method | DPI/PB-14 issue 2 of 2026-01-16 | |
| 20 | Intestines of carnivorous animals | Presence of tapeworms of the genus Echinococcus | SCT method | DPI/PB-13 issue 2 of 2026-01-16 | |
| 21 | Meat samples from animal species susceptible to Trichinella infestation | Presence of Trichinella spp. larvae | Bulk sample leaching using magnetic stirring; Reference method | PN-EN ISO 18743:2015-11 | PN-EN ISO 18743:2015-11/ A1:2024-02 | |
| 22 | Organic fertilizers | Presence of viable eggs of intestinal parasites Ascaris spp., Toxocara spp., Trichuris spp. | Method of isolation, incubation and microscopic observation | PN-Z-19006:2023-04 | |
| 23 | Sewage sludge, material containing sewage sludge | Presence and number of viable eggs of intestinal parasites Ascaris spp., Toxocara spp., Trichuris spp. | Method of isolation, incubation and microscopic observation | PN-Z-19005:2018-10 using I-01/DPI/PN-Z-19005:2018-10 issue 2 of 2026.01.16 | |
| 24 | Consumer products intended for humans including food / fish meat | Presence of Anisakis spp. | Etching method | PN-EN ISO 23036-2:2021-10 | |
| 25 | Trichinella spp. larvae isolates | Presence of Trichinella larvae-specific DNA | PCR method | DPI/PB-16 issue 3 of 2026-01-16 | |
| 26 | Water | Presence of parasitic protozoa of the genera Cryptosporidium and Giardia | Filtration, immunomagnetic separation and direct immunofluorescence method | DPI/PB-17 issue 2 of 2026-01-16 | |
| 27 | Bees | Presence of Varroa destructor mites | Macroscopic method | DPI/PB-43 issue 2 of 2026-01-16 | |
| 28 | Bee brood, bees, honey (sugar food stores), beeswax | Presence of Paenibacillus larvae bacteria | Culture method with biochemical and microscopic confirmation | DPI/PB-44 issue 2 of 2026-01-16 | |
| 29 | Bee brood | Presence of Melissococcus plutonius bacteria | Culture method with microscopic confirmation | DPI/PB-45 issue 2 of 2026-01-16 | |
Reference standards (29)
DNW/PB-01 issue 4 of 2026-03-11
DNW/PB-02 issue 4 of 2026-03-11
DPI/PB-09 issue 3 of 2026-04-21
DPI/PB-12 issue 2 of 2026-01-16
DPI/PB-13 issue 2 of 2026-01-16
DPI/PB-14 issue 2 of 2026-01-16
DPI/PB-16 issue 3 of 2026-01-16
DPI/PB-17 issue 2 of 2026-01-16
DPI/PB-43 issue 2 of 2026-01-16
DPI/PB-44 issue 2 of 2026-01-16
DPI/PB-45 issue 2 of 2026-01-16
DPI/PB-52 issue 2 of 2026-01-16
DPI/PB-53 issue 2 of 2026-01-16
DPI/PB-54 issue 2 of 2026-01-16
DPI/PB-55 issue 2 of 2026-01-16
DPI/PB-56 issue 2 of 2026-01-16
DPI/PB-57 issue 2 of 2026-01-16
DPI/PB-60 issue 2 of 2026-01-16
DPI/PB-61 issue 2 of 2026-01-16
DPI/PB-62 issue 2 of 2026-01-16
DPI/PB-63 issue 2 of 2026-01-16
DPI/PB-64 issue 2 of 2026-01-16
DPI/PB-65 issue 2 of 2026-01-16
DPI/PB-66 issue 2 of 2026-01-16
PN-EN ISO 18743:2015-11
PN-EN ISO 18743:2015-11/ A1:2024-02
PN-EN ISO 23036-2:2021-10
PN-Z-19005:2018-10 using I-01/DPI/PN-Z-19005:2018-10 issue 2 of 2026.01.16
PN-Z-19006:2023-04