Agile and Responsive Structure: A Single Point of Contact for the Entire Project
Information management is as critical as manufacturing quality.
Delays in communication, misalignment between departments, or multiple points of contact can compromise delivery schedules and order compliance — two elements that our clients cannot afford to put at risk.
For this reason SO.L.ME S.R.L. has structured its management process around a simple and powerful principle: a single Project Manager for every contract.
The SO.L.ME Project Manager is your exclusive point of reference for the entire duration of the project. Responsibilities include:
Coordinating all project phases — from definition of technical specifications through delivery and commissioning — guaranteeing continuity and coherence at every step
Managing real-time information — punctual updates on project progress, proactive notification of any critical issues, and rapid response to every technical or documentary request
Interfacing with all internal departments — technical office, production, quality control, and logistics — eliminating the misalignment risks typical of multi-vendor structures
Ensuring compliance with URS and regulatory documentation — with full traceability of every design and constructive decision, essential for IQ/OQ qualification processes in GMP environments
The result is an agile, responsive structure oriented toward results: greater speed, maximum precision.
After-Sales Service: Supporting You Throughout the Equipment Lifecycle
Your relationship with SO.L.ME S.R.L. does not end with equipment delivery.
With us you will never be alone throughout the entire lifecycle of your plants: our after-sales service is structured to guarantee operational continuity, safe use, and full regulatory compliance over time, regardless of the year the equipment was manufactured.
A concrete, documented, and measurable commitment, translated into tangible services supporting technical managers and production directors operating in regulated environments:
Pharmaceutical equipment revamping and retrofitting — technical and regulatory upgrade interventions on existing equipment, to adapt them to new production standards, regulatory requirements, or process needs without bearing the costs of complete replacement
Equipment history archive — we retain the complete technical documentation of every equipment unit manufactured over the last 30 years: construction drawings, material certificates, test records, and all qualification documentation. An information asset that enables rapid, precise, and traceable interventions at any point in the plant’s lifecycle
Real-time spare parts availability — stock availability of principal components and spare parts, to minimize plant downtime and guarantee production continuity for our clients
Programmed periodic maintenance — customized preventive maintenance plans, designed to preserve operational performance and extend equipment service life in compliance with GMP standards and current safety regulations
Safety inspections and non-destructive testing (NDT) — certified periodic inspections to guarantee the structural integrity of pressure equipment, in accordance with the requirements of Pressure Equipment Directive PED 2014/68/UE and ASME certification
OUR MANIFACTURING PROGRAM
Chemical field
Pharmaceutical filed
Maintenance and revamping
Agitation & Mixing Systems
Bespoke Engineering: No Standardized Solutions, No Compromises
Every equipment unit is born from a “bespoke” approach based on the state of the art in constructive technique: no standardized solutions, no compromise between the client’s requirements and the quality of the final result.
Our internal technical office is equipped with the tools and expertise to tackle the most complex design challenges, placing at the disposal of process engineers and technical directors a wealth of consolidated know-how built over more than 40 years of pharmaceutical and chemical plant design:
Design according to calculation codes — we employ the most advanced structural and process calculation software available, compliant with ASME, PED, and international reference standards for the construction of pressure vessels and pressure equipment
Process simulations — we model plant behavior under real operative conditions, enabling optimization of design choices before the construction phase begins
Stress analysis — advanced structural analysis to verify the mechanical integrity of equipment under every operating condition, including startup, shutdown, and emergency scenarios
Laboratory testing — experimental tests and verifications to support design choices, guaranteeing full compliance between the project and expected operational performance
Strict adherence to User Requirement Specifications (URS) — every contract is developed beginning from the user requirements defined by the client, ensuring full compliance with the order from technical specification through final delivery
A rigorous and documented design approach, conceived to meet the needs of clients operating in regulated environments — pharmaceutical, fine chemical, food — where technical precision and documentary traceability are not optional, but essential requirements.
Agile and Responsive Structure: A Single Point of Contact for the Entire Project
Information management is as critical as manufacturing quality.
Delays in communication, misalignment between departments, or multiple points of contact can compromise delivery schedules and order compliance — two elements that our clients cannot afford to put at risk.
For this reason SO.L.ME S.R.L. has structured its management process around a simple and powerful principle: a single Project Manager for every contract.
The SO.L.ME Project Manager is your exclusive point of reference for the entire duration of the project. Responsibilities include:
Coordinating all project phases — from definition of technical specifications through delivery and commissioning — guaranteeing continuity and coherence at every step
Managing real-time information — punctual updates on project progress, proactive notification of any critical issues, and rapid response to every technical or documentary request
Interfacing with all internal departments — technical office, production, quality control, and logistics — eliminating the misalignment risks typical of multi-vendor structures
Ensuring compliance with URS and regulatory documentation — with full traceability of every design and constructive decision, essential for IQ/OQ qualification processes in GMP environments
The result is an agile, responsive structure oriented toward results: greater speed, maximum precision.
After-Sales Service: Supporting You Throughout the Equipment Lifecycle
Your relationship with SO.L.ME S.R.L. does not end with equipment delivery.
With us you will never be alone throughout the entire lifecycle of your plants: our after-sales service is structured to guarantee operational continuity, safe use, and full regulatory compliance over time, regardless of the year the equipment was manufactured.
A concrete, documented, and measurable commitment, translated into tangible services supporting technical managers and production directors operating in regulated environments:
Pharmaceutical equipment revamping and retrofitting — technical and regulatory upgrade interventions on existing equipment, to adapt them to new production standards, regulatory requirements, or process needs without bearing the costs of complete replacement
Equipment history archive — we retain the complete technical documentation of every equipment unit manufactured over the last 30 years: construction drawings, material certificates, test records, and all qualification documentation. An information asset that enables rapid, precise, and traceable interventions at any point in the plant’s lifecycle
Real-time spare parts availability — stock availability of principal components and spare parts, to minimize plant downtime and guarantee production continuity for our clients
Programmed periodic maintenance — customized preventive maintenance plans, designed to preserve operational performance and extend equipment service life in compliance with GMP standards and current safety regulations
Safety inspections and non-destructive testing (NDT) — certified periodic inspections to guarantee the structural integrity of pressure equipment, in accordance with the requirements of Pressure Equipment Directive PED 2014/68/UE and ASME certification
OUR MANIFACTURING PROGRAM
Chemical field
Pharmaceutical filed
Maintenance and revamping
Agitation & Mixing Systems
Constructive Technology and International Certifications: The Foundation of SO.L.ME Quality
The SO.L.ME S.R.L. manufacturing facility is equipped with a modern machinery park that is constantly updated, outfitted with the most advanced welding and forming technologies available on the market. As a further guarantee of constructive precision, we have integrated into our production system an industrial robot dedicated to the automated management of the principal phases of marking, cutting, and welding — a technological choice that translates into greater repeatability, error reduction, and verifiable manufacturing quality at every stage of the process.
The solidity of our quality system is documented by a certification pathway among the most comprehensive and long-standing in the sector:
ISO 9001 — certified since 2002, with over twenty years of continuous management and continuous improvement of the company Quality Management System
Pressure Equipment Directive PED 2014/68/UE — since 2015 we manage and maintain a Total Quality System compliant with the Pressure Equipment Directive, an essential requirement for the construction of pressure equipment destined for the European market
ASME Certification — ASME U Stamp — since 2016 we are authorized by the American ASME body for the design and construction of pressure vessels in accordance with the ASME VIII Div. 1-2 standard (Unfired Pressure Vessels). Our ASME U Stamp pressure vessel qualification enables us to supply certified equipment for clients operating in North American and international markets that adopt this standard as a mandatory constructive requirement
Bespoke Engineering: No Standardized Solutions, No Compromises
Every equipment unit is born from a “bespoke” approach based on the state of the art in constructive technique: no standardized solutions, no compromise between the client’s requirements and the quality of the final result.
Our internal technical office is equipped with the tools and expertise to tackle the most complex design challenges, placing at the disposal of process engineers and technical directors a wealth of consolidated know-how built over more than 40 years of pharmaceutical and chemical plant design:
Design according to calculation codes — we employ the most advanced structural and process calculation software available, compliant with ASME, PED, and international reference standards for the construction of pressure vessels and pressure equipment
Process simulations — we model plant behavior under real operative conditions, enabling optimization of design choices before the construction phase begins
Stress analysis — advanced structural analysis to verify the mechanical integrity of equipment under every operating condition, including startup, shutdown, and emergency scenarios
Laboratory testing — experimental tests and verifications to support design choices, guaranteeing full compliance between the project and expected operational performance
Strict adherence to User Requirement Specifications (URS) — every contract is developed beginning from the user requirements defined by the client, ensuring full compliance with the order from technical specification through final delivery
A rigorous and documented design approach, conceived to meet the needs of clients operating in regulated environments — pharmaceutical, fine chemical, food — where technical precision and documentary traceability are not optional, but essential requirements.
Agile and Responsive Structure: A Single Point of Contact for the Entire Project
Information management is as critical as manufacturing quality.
Delays in communication, misalignment between departments, or multiple points of contact can compromise delivery schedules and order compliance — two elements that our clients cannot afford to put at risk.
For this reason SO.L.ME S.R.L. has structured its management process around a simple and powerful principle: a single Project Manager for every contract.
The SO.L.ME Project Manager is your exclusive point of reference for the entire duration of the project. Responsibilities include:
Coordinating all project phases — from definition of technical specifications through delivery and commissioning — guaranteeing continuity and coherence at every step
Managing real-time information — punctual updates on project progress, proactive notification of any critical issues, and rapid response to every technical or documentary request
Interfacing with all internal departments — technical office, production, quality control, and logistics — eliminating the misalignment risks typical of multi-vendor structures
Ensuring compliance with URS and regulatory documentation — with full traceability of every design and constructive decision, essential for IQ/OQ qualification processes in GMP environments
The result is an agile, responsive structure oriented toward results: greater speed, maximum precision.
After-Sales Service: Supporting You Throughout the Equipment Lifecycle
Your relationship with SO.L.ME S.R.L. does not end with equipment delivery.
With us you will never be alone throughout the entire lifecycle of your plants: our after-sales service is structured to guarantee operational continuity, safe use, and full regulatory compliance over time, regardless of the year the equipment was manufactured.
A concrete, documented, and measurable commitment, translated into tangible services supporting technical managers and production directors operating in regulated environments:
Pharmaceutical equipment revamping and retrofitting — technical and regulatory upgrade interventions on existing equipment, to adapt them to new production standards, regulatory requirements, or process needs without bearing the costs of complete replacement
Equipment history archive — we retain the complete technical documentation of every equipment unit manufactured over the last 30 years: construction drawings, material certificates, test records, and all qualification documentation. An information asset that enables rapid, precise, and traceable interventions at any point in the plant’s lifecycle
Real-time spare parts availability — stock availability of principal components and spare parts, to minimize plant downtime and guarantee production continuity for our clients
Programmed periodic maintenance — customized preventive maintenance plans, designed to preserve operational performance and extend equipment service life in compliance with GMP standards and current safety regulations
Safety inspections and non-destructive testing (NDT) — certified periodic inspections to guarantee the structural integrity of pressure equipment, in accordance with the requirements of Pressure Equipment Directive PED 2014/68/UE and ASME certification
OUR MANIFACTURING PROGRAM
Chemical field
Pharmaceutical filed
Maintenance and revamping
Agitation & Mixing Systems
SO.L.ME S.R.L. — Engineering Excellence in Pharmaceutical, Chemical, and Food Industries
Since 1980, SO.L.ME has designed and manufactured equipment and plants for the pharmaceutical, chemical, and food industries.
With over 40 years of experience and more than 10,000 equipment units delivered, we stand as a consolidated reference point for custom-engineered pharmaceutical and chemical plants, recognized among the leading equipment and plant manufacturers operating in the Italian and international markets.
We are capable of supplying both individual equipment units (tanks, autoclaves, heat exchangers, agitation systems, lenticular filters, drying filters, distillation columns, preparators) and complete automated systems (piping, automation, PLC and process control).
Our organization is furthermore equipped to manage Factory Acceptance Tests (FAT), Site Acceptance Tests (SAT), on-site installation, IQ/OQ qualification, and commissioning both in Italy and internationally.
Design and construction are consistently oriented toward guaranteeing maximum reliability over time and safe operation.
Constructive Technology and International Certifications: The Foundation of SO.L.ME Quality
The SO.L.ME S.R.L. manufacturing facility is equipped with a modern machinery park that is constantly updated, outfitted with the most advanced welding and forming technologies available on the market. As a further guarantee of constructive precision, we have integrated into our production system an industrial robot dedicated to the automated management of the principal phases of marking, cutting, and welding — a technological choice that translates into greater repeatability, error reduction, and verifiable manufacturing quality at every stage of the process.
The solidity of our quality system is documented by a certification pathway among the most comprehensive and long-standing in the sector:
ISO 9001 — certified since 2002, with over twenty years of continuous management and continuous improvement of the company Quality Management System
Pressure Equipment Directive PED 2014/68/UE — since 2015 we manage and maintain a Total Quality System compliant with the Pressure Equipment Directive, an essential requirement for the construction of pressure equipment destined for the European market
ASME Certification — ASME U Stamp — since 2016 we are authorized by the American ASME body for the design and construction of pressure vessels in accordance with the ASME VIII Div. 1-2 standard (Unfired Pressure Vessels). Our ASME U Stamp pressure vessel qualification enables us to supply certified equipment for clients operating in North American and international markets that adopt this standard as a mandatory constructive requirement
Bespoke Engineering: No Standardized Solutions, No Compromises
Every equipment unit is born from a “bespoke” approach based on the state of the art in constructive technique: no standardized solutions, no compromise between the client’s requirements and the quality of the final result.
Our internal technical office is equipped with the tools and expertise to tackle the most complex design challenges, placing at the disposal of process engineers and technical directors a wealth of consolidated know-how built over more than 40 years of pharmaceutical and chemical plant design:
Design according to calculation codes — we employ the most advanced structural and process calculation software available, compliant with ASME, PED, and international reference standards for the construction of pressure vessels and pressure equipment
Process simulations — we model plant behavior under real operative conditions, enabling optimization of design choices before the construction phase begins
Stress analysis — advanced structural analysis to verify the mechanical integrity of equipment under every operating condition, including startup, shutdown, and emergency scenarios
Laboratory testing — experimental tests and verifications to support design choices, guaranteeing full compliance between the project and expected operational performance
Strict adherence to User Requirement Specifications (URS) — every contract is developed beginning from the user requirements defined by the client, ensuring full compliance with the order from technical specification through final delivery
A rigorous and documented design approach, conceived to meet the needs of clients operating in regulated environments — pharmaceutical, fine chemical, food — where technical precision and documentary traceability are not optional, but essential requirements.
Agile and Responsive Structure: A Single Point of Contact for the Entire Project
Information management is as critical as manufacturing quality.
Delays in communication, misalignment between departments, or multiple points of contact can compromise delivery schedules and order compliance — two elements that our clients cannot afford to put at risk.
For this reason SO.L.ME S.R.L. has structured its management process around a simple and powerful principle: a single Project Manager for every contract.
The SO.L.ME Project Manager is your exclusive point of reference for the entire duration of the project. Responsibilities include:
Coordinating all project phases — from definition of technical specifications through delivery and commissioning — guaranteeing continuity and coherence at every step
Managing real-time information — punctual updates on project progress, proactive notification of any critical issues, and rapid response to every technical or documentary request
Interfacing with all internal departments — technical office, production, quality control, and logistics — eliminating the misalignment risks typical of multi-vendor structures
Ensuring compliance with URS and regulatory documentation — with full traceability of every design and constructive decision, essential for IQ/OQ qualification processes in GMP environments
The result is an agile, responsive structure oriented toward results: greater speed, maximum precision.
After-Sales Service: Supporting You Throughout the Equipment Lifecycle
Your relationship with SO.L.ME S.R.L. does not end with equipment delivery.
With us you will never be alone throughout the entire lifecycle of your plants: our after-sales service is structured to guarantee operational continuity, safe use, and full regulatory compliance over time, regardless of the year the equipment was manufactured.
A concrete, documented, and measurable commitment, translated into tangible services supporting technical managers and production directors operating in regulated environments:
Pharmaceutical equipment revamping and retrofitting — technical and regulatory upgrade interventions on existing equipment, to adapt them to new production standards, regulatory requirements, or process needs without bearing the costs of complete replacement
Equipment history archive — we retain the complete technical documentation of every equipment unit manufactured over the last 30 years: construction drawings, material certificates, test records, and all qualification documentation. An information asset that enables rapid, precise, and traceable interventions at any point in the plant’s lifecycle
Real-time spare parts availability — stock availability of principal components and spare parts, to minimize plant downtime and guarantee production continuity for our clients
Programmed periodic maintenance — customized preventive maintenance plans, designed to preserve operational performance and extend equipment service life in compliance with GMP standards and current safety regulations
Safety inspections and non-destructive testing (NDT) — certified periodic inspections to guarantee the structural integrity of pressure equipment, in accordance with the requirements of Pressure Equipment Directive PED 2014/68/UE and ASME certification
OUR MANIFACTURING PROGRAM
Chemical field
Pharmaceutical filed
Maintenance and revamping