Revolutionizing Regulated Industries: Unleashing the Power of aPaaS with COTS and Low-Code Platforms

dc1143be

In the ever-evolving landscape of regulated industries such as life sciences, pharmaceutical manufacturing, gene therapy and medical devices; the demand for cutting-edge technology solutions is paramount. As these sectors strive for innovation while adhering to stringent regulations as per electronic records guidelines defined in US FDA 21 CFR Part 11, EU Annexure 11 and GAMP 5 category standards; it becomes imperative to explore platforms that can seamlessly blend customization features with efficiency and provide integration among business processes.

The regulated companies have finely leveraged cloud technology to streamline business activities that address current cyber security challenges and provide customized solutions. These service offerings consist mainly of Software-as-a-Service (SaaS) and Platform-as-a-Service (PaaS). But more often than not, these companies require customized solutions for their unique needs instead of just standard solutions. Now, before delving into the same let’s first understand what are cloud solutions and their types.

Cloud solutions refer to computing services and resources delivered over the internet, commonly known as the cloud. These services include a variety of applications, storage, processing power, and more, enabling users to access and use these resources remotely rather than on their local devices or servers.

Public and Private

A private cloud is hosted, used and maintained by a single organization. This means it is a dedicated cloud that is solely used by an individual company who has overall control over the infrastructure and its services.

Ensures complete autonomy.

  • They can customize the environment according to their own needs.
  • Companies meet their compliance requirements better.
  • Higher security and reduced chances of cyber attacks since data is not shared, chances of security breaches are reduced significantly.

Public cloud is a third-party managed platform that is used by multiple companies to do their regular tasks. This setting relieves companies from owning or maintaining their own infrastructure. Public cloud resources usually include virtual machines, applications and storage.

  • Cost effective as companies don’t have to maintain their own infrastructure.
  • Offers higher agility and scalability, can increase or decrease resources as required without impact of increasing or decreasing workload and fluctuation in business requirements.
  • Promotes efficiency.
  • Pay for what you use.

Types of Cloud Models

Broadly there are three types of cloud models:

  • In the IaaS (Infrastructure as a Service) model, vendors offer the entire cloud infrastructure including hardware, computing resources and data centres. This way the end user can access the hardware over the internet while paying for the service. Usually, companies sign up for virtual machines or they go for a dedicated hardware for their personal usage.
  • In the PaaS (Platform as a Service) model, vendors provide users with a development and deployment environment where clients build their own applications and software. PaaS is a great solution for businesses who want personalized softwares. A low to no code environment additionally helps companies build applications with no prior knowledge of programming languages.
  • Among the three Cloud models, SaaS (Software as a Service) is by far the most popular! In this model, companies offer their own software or applications to clients. It is the vendor who then takes care of the maintenance of these software. They are also responsible for the updates. Users get generic applications with SaaS.
Img1

Irrespective of SaaS’ high demand, regulated industries seek personalized solutions. As new technologies seep in every day, a sub-model of PaaS – aPaaS – outshines as a better alternative for automating highly regulated industries. Let’s look at this article to explore the benefits of adopting an Application-Platform-as-a-Service (aPaaS) solution over traditional Software-as-a-Service (SaaS) model, highlighting the advantages and proposing a novel approach – aPaaS with Commercial Off-The-Shelf (COTS) products – for enhanced adaptability, time efficiency, cost management and building of business-centric solutions without developing them from scratch.

Challenges with SaaS in Regulated Industries

1. Customization Roadblocks: Traditional SaaS solutions often come with predefined features and limited flexibility, creating roadblocks for organizations in regulated industries such as in the lifesciences, pharmaceuticals, and medical devices that have unique workflows and compliance requirements such as US FDA 21 CFR Part 11, EU Annexure 1, GAMP 4 & 5 category standards. Although in private cloud, customization is possible but comes with very high cost and maintenance.

2. Limited Control Over Updates: In regulated environments, controlling the timing and impact of software updates is crucial. SaaS solutions may force updates that can disrupt workflows. To ensure processes run smoothly and as expected companies need to validate the updates which is pretty time consuming and shoots up costs.

SaaS Advantages and Disadvantages
SaaS Advantages and Disadvantages

3. Integration Issues: No service provider typically offers a comprehensive suite of SaaS products that fully meet a business’s diverse needs. This leads organizations to depend on multiple SaaS providers, resulting in the management of multiple accounts and an associated high cost of integration.

4. Added Costs: Services from multiple vendors for different products also involve additional costs. Additionally, standard Service Level Agreements (SLAs) offered by SaaS providers may not be sufficient for regulated environments, requiring negotiations for enhanced uptime, security, and data recovery guarantees, which would be an added cost to the organisations. This is a key issue as every company runs on a specific budget.

The Essence of aPaaS in Regulated Industries

1. aPaaS as a Subset of PaaS
Recognizing aPaaS as a subset of Platform as a Service (PaaS) sheds light on its specialized role in providing tailored solutions for application development. aPaaS providers leverage Low Code No Code (LCNC) methodologies, making application development more accessible and efficient.

2. LCNC Methodology
The LCNC methodology empowers businesses to rapidly develop applications, reducing time-to-market. By offering Low Code platforms on their cloud infrastructure, service providers facilitate the creation of customized applications without the need for extensive coding expertise.

aPaaS features

3. Customization Benefits
One of the key advantages of developing products on such Low Code platforms is the flexibility they offer to accommodate customer-specific requirements. This adaptability is particularly beneficial when organizations seek tailored solutions to meet their unique business needs, enabling a more agile response to changing market dynamics. Users get this advantage when they opt for an aPaaS platform.

4. Deployment Methods

There are two ways of deploying an aPaaS platform:

  • On Cloud: Usually, aPaaS vendors deliver Low Code platforms on their own cloud infrastructure. In this case the vendor is responsible for maintaining the platform and infrastructure. Users can leverage the platform to build applications of their own choice.
  • On-Premise: For organizations with existing data centers and virtual servers, hosting Low Code platforms (aPaaS) on-premise is a viable option. In this scenario, businesses assume responsibility for managing the infrastructure while the service provider offers platform support. Therefore, businesses are more accountable for the application created and their performance is heavily dependent on the on-premise infrastructure.

Advantages of aPaaS in Regulated Industries:

1. Tailored Solutions: aPaaS empowers organizations to build custom applications tailored to their unique needs. This is particularly advantageous in regulated industries such as lifesciences, pharmaceuticals, and medical devices where workflows can be complex and must align with strict guidelines.

2. Reduced Compliance Burden: aPaaS solutions for life sciences, pharmaceutical manufacturing, gene therapy and medical devices must comply with regulations such as US FDA 21 CFR Part 11, EU Annexure 11, GAMP 5 category standards, HIPAA, SOC 2 etc. Many aPaaS platforms include pre-built compliance features and frameworks. This allows organizations in regulated industries to quickly and easily ensure their applications meet compliance requirements. This can significantly reduce the burden of compliance for regulated organizations.

3. Greater Control Over Data: With aPaaS, organizations retain greater control over their data, facilitating compliance with industry regulations.

4. Efficient Integration with Existing Systems: aPaaS solutions allow seamless integration with existing systems, fostering interoperability, and reducing disruptions during the adoption phase. This is crucial for industries where legacy systems are prevalent. Also, multiple applications are integrated on a single platform that work by sharing data. This helps in seamless business proceedings.

5. Reduced Cost: With aPaaS, development teams can leverage pre-built modules, components, and templates. This accelerates the application development process, saving time and reducing the overall development cost.

6. Time Efficiency: Ready-made functionalities provided by aPaaS platforms eliminate the need for coding from scratch. Developers can focus on customizing these components, significantly reducing the time required to bring an application to market.

COTS in the Mix

Understanding COTS: Commercial Off-The-Shelf (COTS) products are ready-to-use applications that vendors usually offer on top of a low code platform (aPaaS). COTS on Lowcode helps subside all disadvantages where only the benefits can be reaped.
Deployment Method: COTS products or applications are deployed on a customer’s infrastructure. When hosted on service providers’ clouds, they fall under the category of Software as a Service (SaaS).
Customization Benefits: COTS products (applications) offered by vendors on Low Code platforms provide customers the flexibility to accommodate customer-specific requirements. This synergy allows for tailored solutions that align with the unique needs of regulated industries.

Some examples of COTS are eQMS, DMS, LMS, LIMS, RIMS etc.

Proposing aPaaS with COTS

Proposing aPaaS with COTS

1. Standard Products with Customization Benefits: aPaaS with COTS products (applications) offers the dual advantage of getting ready-made solutions with the flexibility of customized development. Organizations can use COTS for standard processes and easily customize with aPaaS when needed. aPaaS allows them to develop custom add-ons or extensions that add functionality to existing COTS solutions.

2. Cost-Effective Scalability: Leveraging COTS for standard functionalities reduces development costs, while aPaaS facilitates cost-effective customization. This hybrid model ensures scalability without compromising budget constraints.

3. Streamlined Compliance: COTS products often come with built-in compliance features. Integrating them with aPaaS allows organizations to extend these features to custom applications, ensuring a streamlined approach to compliance and regulatory adherence.

4. Rapid Development and Deployment: The combination of aPaaS with COTS enables rapid development and deployment of applications. This agility is crucial in regulated industries where timely responses to changing requirements are essential.

aPaas COTS offerings

5. Efficient Integration: aPaaS providers can consolidate various services under a single platform streamlining integration, reducing complexity and overall costs. Applications in this case is integrated using API (Application Programming Interfaces) that helps in exchange of data and performance of key tasks. For example, a Quality Management System (QMS) can easily ensure if a person is trained to do a work by its integration with a Learning Management System (LMS) hosted in aPaaS.

As regulated industries continue to navigate the delicate balance between innovation and compliance, the adoption of aPaaS with COTS emerges as a strategic move. This approach not only addresses the limitations of traditional SaaS models but also provides a tailored, cost-effective, and scalable solution. By embracing aPaaS with COTS, regulated industries such as life sciences, pharmaceutical manufacturing, gene therapy and medical devices propel themselves into a realm where technology serves as an enabler, not a restriction. So, are you ready to unlock efficiency and embrace a future where compliance and innovation coexist harmoniously? The time is now. Achieve business process excellence using aPaaS with COTS solutions.

Schedule a Free Consultation
Request a Demo
Articles

See More Articles
eQMS

Root Cause Analysis with example for “5” Why technique

Root Cause Analysis (RCA) is a method that is used to address a problem or non-conformance in the quality process to get to the “root cause” (actual cause of origin) of the non-conformity. RCA helps to correct or eliminate the cause and prevent the problem from recurring (preventive action). Root cause analyses is aimed at improving products or processes quality and must an in systematic ways to be effective. Different Methods of doing Root Cause Analysis: Root Cause Analysis Methodology   Fish bone technique The “5” Why’s technique. Barrier Analysis Change Analysis Casual Factor tree analysis Failure mode and effects analysis Pareto analysis Advantages: To identify non-conformity and the causes, so that permanent solution can be found. To develop a logical approach of problem-solving, using data that already exists in QMS (Quality Management System) To identify current and also future needs for organizational quality improvement. To establish a repeatable systematic step by step processes, in which one process can confirm the results of another with deep analysis. Challenges: Not having the ability to understand the problem and therefore not defining it correctly. Not considering all possible failure modes. Not able to identify all root causes. No proper defined solution for the non-conformity. The “5” Why technique causes mapping Non-conformity identified: Decrease in the viscosity of Vitamin D3 syrup. The “5” why technique can be expanded to 15 why or 150 why the deeper you go the more thorough analyzing takes place and reveals better solutions Contact us for more information about the AmpleLogic Quality Systems Offerings.   Schedule a Free Consultation Request a Demo First NameLast NameCompany NameEmailPhone NumberDesignationCountrySelect CountryAfghanistanAland IslandsAlbaniaAlgeriaAmerican SamoaAndorraAngolaAnguillaAntarcticaAntigua and BarbudaArgentinaArmeniaArubaAustraliaAustriaAzerbaijanBahamasBahrainBangladeshBarbadosBelarusBelauBelgiumBelizeBeninBermudaBhutanBoliviaBonaire, Saint Eustatius and SabaBosnia and HerzegovinaBotswanaBouvet IslandBrazilBritish Indian Ocean TerritoryBritish Virgin IslandsBruneiBulgariaBurkina FasoBurundiCambodiaCameroonCanadaCape VerdeCayman IslandsCentral African RepublicChadChileChinaChristmas IslandCocos (Keeling) IslandsColombiaComorosCook IslandsCosta RicaCroatiaCubaCuraçaoCyprusCzech RepublicDemocratic Republic of the Congo (Kinshasa)DenmarkDjiboutiDominicaDominican RepublicEcuadorEgyptEl SalvadorEquatorial GuineaEritreaEstoniaEthiopiaFalkland IslandsFaroe IslandsFijiFinlandFranceFrench GuianaFrench PolynesiaFrench Southern TerritoriesGabonGambiaGeorgiaGermanyGhanaGibraltarGreeceGreenlandGrenadaGuadeloupeGuamGuatemalaGuernseyGuineaGuinea-BissauGuyanaHaitiHeard Island and McDonald IslandsHondurasHong KongHungaryIcelandIndiaIndonesiaIranIraqIrelandIsle of ManIsraelItalyIvory CoastJamaicaJapanJerseyJordanKazakhstanKenyaKiribatiKosovoKuwaitKyrgyzstanLaosLatviaLebanonLesothoLiberiaLibyaLiechtensteinLithuaniaLuxembourgMacao S.A.R., ChinaMacedoniaMadagascarMalawiMalaysiaMaldivesMaliMaltaMarshall IslandsMartiniqueMauritaniaMauritiusMayotteMexicoMicronesiaMoldovaMonacoMongoliaMontenegroMontserratMoroccoMozambiqueMyanmarNamibiaNauruNepalNetherlandsNew CaledoniaNew ZealandNicaraguaNigerNigeriaNiueNorfolk IslandNorth KoreaNorthern Mariana IslandsNorwayOmanPakistanPalestinian TerritoryPanamaPapua New GuineaParaguayPeruPhilippinesPitcairnPolandPortugalPuerto RicoQatarRepublic of the Congo (Brazzaville)ReunionRomaniaRussiaRwandaSaint BarthélemySaint HelenaSaint Kitts and NevisSaint LuciaSaint Martin (Dutch part)Saint Martin (French part)Saint Pierre and MiquelonSaint Vincent and the GrenadinesSamoaSan MarinoSao Tome and PrincipeSaudi ArabiaSenegalSerbiaSeychellesSierra LeoneSingaporeSlovakiaSloveniaSolomon IslandsSomaliaSouth AfricaSouth Georgia/Sandwich IslandsSouth KoreaSouth SudanSpainSri LankaSudanSurinameSvalbard and Jan MayenSwazilandSwedenSwitzerlandSyriaTaiwanTajikistanTanzaniaThailandTimor-LesteTogoTokelauTongaTrinidad and TobagoTunisiaTurkeyTurkmenistanTurks and Caicos IslandsTuvaluUgandaUkraineUnited Arab EmiratesUnited Kingdom (UK)United States (US)United States (US) Minor Outlying IslandsUnited States (US) Virgin IslandsUruguayUzbekistanVanuatuVaticanVenezuelaVietnamWallis and FutunaWestern SaharaYemenZambiaZimbabweWhere you heard about us?– Select –Google SearchLinkedInReferralWord of MouthLinkedIn AdsMediumRequirementGet in touch

Learn more
DMS

Why is embracing the Document Management System still intimidating?

DMS in a layperson perception A thorough-cum-simpler explanation of Document Management System will make us understand about the efficacy of this digital trend. With the name “Electronic Document Management System”, we get an overall idea that the system is supposedly managing the documentation process. Now, this process is the common one being done in every organization, we all know. Here the point comes is : How are these documentation things being processed or managed in various industries these days? Collecting all the needed data or information of a company and putting them down in a specific file or document is something that we know very well, which has been done manually for ages. But with trending technological inventions like IoT, AI, Cyber Security, etc., in the ongoing digital world, we must step up to a more effort-less mode of documentation. So, with this, we came up with eDMS.  Replacing manual documentation work to automated-cum-electronic documentation, Electronic Document Management System has brought a different level of changes in contemporary pharma as well as life sciences companies. A quick peek of digitalization using Electronic Document Management Software (eDMS) While DMS has given us chances to ease our pain with an effective modification in documentation tasks, FDA’s 21 CFR part 11 has confirmed that electronic documents along with the records and signatures can surely be considered as the legitimate ones. Hence, it has confirmed that there will be no difference between paper signature and e-signature, rather the later one will be more considerable. Let’s have a quick walk through the benefits we have gained with Electronic Document Management System in contemporary pharma companies. Easy creation, management, and storage of all the crucial data and information of the company is possible with DMS. On incorrect data feeding, mismatch of information, missing data, you will get a reminder or notification which is not possible in manual management. All the data is stored in a specific and common cloud, which is accessible to everyone from everywhere. A smooth documentation now ensures a streamline workflow and saves a lot of time and resources which can be used in other areas of growth. Complete replacement of paperworks into paperless documentation becomes easy with eDMS. Having thorough data on drugs, research, new compliances, regulations require error-free documentation and with Pharmaceutical Document Management Solution this task can be managed easily. Storage of all the digital documents under a common cloud is much safer than keeping manual data in the form of documents stored in some physical storage. Accessible cloud storage documentation allows you to access the data whenever and wherever required, whereas in manual management there is some chance of missing out on important data. An organized documentation not only takes care of the data storage but also ensures a smooth flow of additional departments like SOP Management, manufacturing, operation, quality planning, etc. Terrorizing reasons restricting full-fledged eDMS inculcation Despite a lot of benefits, there are many companies who are reconsidering their decisions of incorporating Document Management Systems into their business. Every innovation comes with certain pros and cons. When we have already understood several benefits of the automatic documentation process, let’s explore the risky or stressed side or probable challenges of this digital trend. Data being vulnerable: With documentation being staged on digital platforms, it is extremely necessary to keep an eye on the security side. When crucial data is stored in the cloud then there comes a major terror of data being vulnerable and being attacked by malicious cyber frauds. Hence, it is required to maintain utmost cybersecurity ensuring the documentation is safe in the cloud kept away from cyber thefts. Doubt on successful implementation: There are so many growing features of Electronic Document Management and Tracking Software for Lifesciences industries, but we need to explore all those specifications accurately. Adding on a digital trend to a business could sound fun, but the real game starts when you implement the software effectively. This can be done with active seminars, group discussions, and taking feedback from employees (who are using it) on document management solution. Fear of smooth integration: The DMS must come up with appropriate integration of all relevant departments, then only we can assure its potential usage. Hence integration of DMS with other in-house applications must be done properly to make the system work automatically and independently. Staying inconsistent in usage: To replace paperworks with digital paperless ones, giving employees detailed training on Pharmaceutical Document Management and Tracking Software is essential. Hence, keeping the usage of DMS consistent becomes a tough task if the users are not well-trained. So, the prior task is to train employees about the usage of the platform and bring consistency in keeping the system in work consistently. Realising the probable challenges as well as conquered benefits of Document Management Solution we can easily understand how to proceed with this amazing transformation from loads of paper-based documents to hassle-free paperless one-stop-data centres. AmpleLogic’s best DMS software is assisting several pharma as well as other businesses to successfully implement this amazing digital tweak to their work processes making lives easier. Talk to our team to enroll for a free demo on Electronic Document Management System. Schedule a Free Consultation Request a Demo First NameLast NameCompany NameEmailPhone NumberDesignationCountrySelect CountryAfghanistanAland IslandsAlbaniaAlgeriaAmerican SamoaAndorraAngolaAnguillaAntarcticaAntigua and BarbudaArgentinaArmeniaArubaAustraliaAustriaAzerbaijanBahamasBahrainBangladeshBarbadosBelarusBelauBelgiumBelizeBeninBermudaBhutanBoliviaBonaire, Saint Eustatius and SabaBosnia and HerzegovinaBotswanaBouvet IslandBrazilBritish Indian Ocean TerritoryBritish Virgin IslandsBruneiBulgariaBurkina FasoBurundiCambodiaCameroonCanadaCape VerdeCayman IslandsCentral African RepublicChadChileChinaChristmas IslandCocos (Keeling) IslandsColombiaComorosCook IslandsCosta RicaCroatiaCubaCuraçaoCyprusCzech RepublicDemocratic Republic of the Congo (Kinshasa)DenmarkDjiboutiDominicaDominican RepublicEcuadorEgyptEl SalvadorEquatorial GuineaEritreaEstoniaEthiopiaFalkland IslandsFaroe IslandsFijiFinlandFranceFrench GuianaFrench PolynesiaFrench Southern TerritoriesGabonGambiaGeorgiaGermanyGhanaGibraltarGreeceGreenlandGrenadaGuadeloupeGuamGuatemalaGuernseyGuineaGuinea-BissauGuyanaHaitiHeard Island and McDonald IslandsHondurasHong KongHungaryIcelandIndiaIndonesiaIranIraqIrelandIsle of ManIsraelItalyIvory CoastJamaicaJapanJerseyJordanKazakhstanKenyaKiribatiKosovoKuwaitKyrgyzstanLaosLatviaLebanonLesothoLiberiaLibyaLiechtensteinLithuaniaLuxembourgMacao S.A.R., ChinaMacedoniaMadagascarMalawiMalaysiaMaldivesMaliMaltaMarshall IslandsMartiniqueMauritaniaMauritiusMayotteMexicoMicronesiaMoldovaMonacoMongoliaMontenegroMontserratMoroccoMozambiqueMyanmarNamibiaNauruNepalNetherlandsNew CaledoniaNew ZealandNicaraguaNigerNigeriaNiueNorfolk IslandNorth KoreaNorthern Mariana IslandsNorwayOmanPakistanPalestinian TerritoryPanamaPapua New GuineaParaguayPeruPhilippinesPitcairnPolandPortugalPuerto RicoQatarRepublic of the Congo (Brazzaville)ReunionRomaniaRussiaRwandaSaint BarthélemySaint HelenaSaint Kitts and NevisSaint LuciaSaint Martin (Dutch part)Saint Martin (French part)Saint Pierre and MiquelonSaint Vincent and the GrenadinesSamoaSan MarinoSao Tome and PrincipeSaudi ArabiaSenegalSerbiaSeychellesSierra LeoneSingaporeSlovakiaSloveniaSolomon IslandsSomaliaSouth AfricaSouth Georgia/Sandwich IslandsSouth KoreaSouth SudanSpainSri LankaSudanSurinameSvalbard and Jan MayenSwazilandSwedenSwitzerlandSyriaTaiwanTajikistanTanzaniaThailandTimor-LesteTogoTokelauTongaTrinidad and TobagoTunisiaTurkeyTurkmenistanTurks and Caicos IslandsTuvaluUgandaUkraineUnited Arab EmiratesUnited Kingdom (UK)United States (US)United States (US) Minor Outlying IslandsUnited States (US) Virgin IslandsUruguayUzbekistanVanuatuVaticanVenezuelaVietnamWallis and FutunaWestern SaharaYemenZambiaZimbabweWhere you heard about us?– Select –Google

Learn more
LMS

Benefits of Training Management System

Here’s what a Training Management System can, and should, do for you: Learning Management System makes it very easy for trainers to update existing training content or add new content in a short time Comply and Meet essential regulatory requirements and other best practices more easily Enhance managers and employees ability to achieve required results, not just complete the training Measure the reduction in operational expenses, travel time and on-site visits Reduce the time for needed for creating, updating, printing and shipping of learning course manuals and documentation Dramatically reduce the cost of software for managing and creating training courses Improve the administration of your learning programs Increase your ability to manage and deploy e-learning to your employees across any location Consolidates training information to improve efficiency, improved facilities coordination and cost utilization Improve personnel performance by enabling you to manage admiration and human resources more effectively Implement more and more effective skills and competency training management programs Reduce training costs Increase the number of training courses that you can deliver for less money Training Course materials on an effectively deployed Learning Management System (LMS) can be accessed by employees across geographies, without affecting the quality or consistency of training These training systems allow the creation, personalization, and download of detailed training reports outlining the progress of the learners, departmental groups, completion of work, time taken to complete the task, etc. which allows easy evaluation of their progress either as an individual or a group A modern Learning Management System, like AmpleLogic LMS, can support your organizations as it grows, and give you the flexibility to add the latest features and functionality to support your training and learning programs Are you ready to invest in a new Learning Management System or LMS? Contact us today to find out more or schedule a demo. Schedule a Free Consultation Request a Demo First NameLast NameCompany NameEmailPhone NumberDesignationCountrySelect CountryAfghanistanAland IslandsAlbaniaAlgeriaAmerican SamoaAndorraAngolaAnguillaAntarcticaAntigua and BarbudaArgentinaArmeniaArubaAustraliaAustriaAzerbaijanBahamasBahrainBangladeshBarbadosBelarusBelauBelgiumBelizeBeninBermudaBhutanBoliviaBonaire, Saint Eustatius and SabaBosnia and HerzegovinaBotswanaBouvet IslandBrazilBritish Indian Ocean TerritoryBritish Virgin IslandsBruneiBulgariaBurkina FasoBurundiCambodiaCameroonCanadaCape VerdeCayman IslandsCentral African RepublicChadChileChinaChristmas IslandCocos (Keeling) IslandsColombiaComorosCook IslandsCosta RicaCroatiaCubaCuraçaoCyprusCzech RepublicDemocratic Republic of the Congo (Kinshasa)DenmarkDjiboutiDominicaDominican RepublicEcuadorEgyptEl SalvadorEquatorial GuineaEritreaEstoniaEthiopiaFalkland IslandsFaroe IslandsFijiFinlandFranceFrench GuianaFrench PolynesiaFrench Southern TerritoriesGabonGambiaGeorgiaGermanyGhanaGibraltarGreeceGreenlandGrenadaGuadeloupeGuamGuatemalaGuernseyGuineaGuinea-BissauGuyanaHaitiHeard Island and McDonald IslandsHondurasHong KongHungaryIcelandIndiaIndonesiaIranIraqIrelandIsle of ManIsraelItalyIvory CoastJamaicaJapanJerseyJordanKazakhstanKenyaKiribatiKosovoKuwaitKyrgyzstanLaosLatviaLebanonLesothoLiberiaLibyaLiechtensteinLithuaniaLuxembourgMacao S.A.R., ChinaMacedoniaMadagascarMalawiMalaysiaMaldivesMaliMaltaMarshall IslandsMartiniqueMauritaniaMauritiusMayotteMexicoMicronesiaMoldovaMonacoMongoliaMontenegroMontserratMoroccoMozambiqueMyanmarNamibiaNauruNepalNetherlandsNew CaledoniaNew ZealandNicaraguaNigerNigeriaNiueNorfolk IslandNorth KoreaNorthern Mariana IslandsNorwayOmanPakistanPalestinian TerritoryPanamaPapua New GuineaParaguayPeruPhilippinesPitcairnPolandPortugalPuerto RicoQatarRepublic of the Congo (Brazzaville)ReunionRomaniaRussiaRwandaSaint BarthélemySaint HelenaSaint Kitts and NevisSaint LuciaSaint Martin (Dutch part)Saint Martin (French part)Saint Pierre and MiquelonSaint Vincent and the GrenadinesSamoaSan MarinoSao Tome and PrincipeSaudi ArabiaSenegalSerbiaSeychellesSierra LeoneSingaporeSlovakiaSloveniaSolomon IslandsSomaliaSouth AfricaSouth Georgia/Sandwich IslandsSouth KoreaSouth SudanSpainSri LankaSudanSurinameSvalbard and Jan MayenSwazilandSwedenSwitzerlandSyriaTaiwanTajikistanTanzaniaThailandTimor-LesteTogoTokelauTongaTrinidad and TobagoTunisiaTurkeyTurkmenistanTurks and Caicos IslandsTuvaluUgandaUkraineUnited Arab EmiratesUnited Kingdom (UK)United States (US)United States (US) Minor Outlying IslandsUnited States (US) Virgin IslandsUruguayUzbekistanVanuatuVaticanVenezuelaVietnamWallis and FutunaWestern SaharaYemenZambiaZimbabweWhere you heard about us?– Select –Google SearchLinkedInReferralWord of MouthLinkedIn AdsMediumRequirementGet in touch

Learn more