How to Train a Foundational Model
with Custom Datasets
Tech Deep Dives • April 14, 2025
We cover best practices in preprocessing, hyperparameter tuning, and evaluation –
to build an AI that truly
understands your unique domain.

Training a foundation model (a large AI model like a transformer trained on broad data) with custom, domain-specific datasets is increasingly crucial for cutting-edge applications in healthcare and life sciences. General-purpose models (e.g., GPT-style LLMs) are powerful but may not capture the specialized terminology, context, and regulatory constraints of medical or pharmaceutical data. By leveraging domain-specific data, organizations can create models that deeply understand biomedical language and nuance.
For example, a model like BioBERT, which was pre-trained on biomedical literature, significantly outperforms the original BERT on biomedical tasks such as named entity recognition and question answering ( BioBERT: a pre-trained biomedical language representation model for biomedical text mining - PubMed ). This demonstrates that pretraining on in-domain data yields tangible performance gains, enabling more accurate and relevant AI behavior in specialized fields. In an industry where accuracy can be life-critical, customizing foundation models with the right data is a strategic imperative.
The Importance of Domain-Specific Data in Healthcare AI
Domain-specific data imbues a foundation model with knowledge that generic training cannot provide. Medical and scientific texts contain unique jargon (e.g., “ECG,” “oncogene”) and structured formats that a general model might not fully grasp. Fine-tuning or pretraining on industry-specific terminology (like medical journals, clinical trial reports, or EHR notes) helps the model internalize those concepts.
This is especially important in healthcare, where understanding context and rare terms (e.g. rare diseases or drug names) is crucial. A general model might treat “madras” as a city or fabric, but a domain-trained model knows “MADRAS” could refer to a disease acronym in a clinical context. Moreover, domain data ensures the model reflects real-world scenarios and distributions relevant to pharma – for instance, learning the typical structure of lab reports or the way physicians phrase diagnoses. By training on data that mirrors the target use cases, the foundation model becomes not just a language expert, but an expert in the language of healthcare, leading to better results. Studies confirm that a model adapted to biomedical corpora can understand complex medical texts better and yield higher accuracy on healthcare tasks ( BioBERT: a pre-trained biomedical language representation model for biomedical text mining - PubMed ).
However, quality and diversity of the custom dataset are paramount. If the data is narrow or biased, the model will inherit those limitations. Pharma innovators should seek datasets that cover a range of patient demographics, conditions, and text styles (clinical notes, research papers, regulatory documents) to avoid blind spots. The risk of bias and health disparities must be managed by including data from diverse populations – a lesson learned from prior algorithms that performed poorly on underrepresented groups ( Ethical data acquisition for LLMs and AI algorithms in healthcare - PMC ). In essence, assembling a rich, representative corpus of domain data is the foundation for a high-performing model.
Sourcing and Preparing High-Quality Data
Building a custom dataset begins with data sourcing. In healthcare and life sciences, valuable data sources include electronic health records (EHRs), clinical trial databases, scientific publications, drug discovery data (e.g. chemical structures, genomic data), and even patient-generated data (surveys, device readings). Much of this data is sensitive and siloed. Organizations should establish partnerships (e.g. with hospitals or research networks) and data-sharing agreements that allow use of anonymized data for AI development. Public datasets can help bootstrap a project – for instance, using PubMed abstracts or open clinical datasets – but proprietary internal data often gives the competitive edge. It’s wise to combine multiple sources: for example, merging textual data from research articles with real-world clinical notes can give a model both formal medical knowledge and informal colloquial patterns.
Before training, all data should be standardized and cleaned: formats unified (converting all to a common structure), medical abbreviations expanded or clarified, and errors or inconsistencies corrected. Data cleaning also means removing duplicates and correcting mislabeled entries to ensure the model isn’t learning from noise.
A crucial step is data de-identification for any patient information. All personally identifiable information (names, addresses, IDs) and protected health information must be removed or encoded to meet regulations like HIPAA. In practice, this might involve using automated de-identification tools on EHR text and having human reviewers verify that no patient can be re-identified. For EHR foundation models, adopting measures such as training on data de-identified to HIPAA standards and obtaining necessary patient consent is non-negotiable. By training only on data that has been stripped of direct identifiers, we reduce the risk of the model memorizing any individual's data. At the same time, maintaining the statistical distribution of the data (through techniques like differential privacy) can allow learning from patient records without compromising privacy.
Annotation and labeling are additional considerations, especially if you plan to fine-tune the foundational model for specific tasks. Domain-specific data often requires precise labeling by experts. For example, if building a clinical entity extractor, you may need physicians to annotate symptoms and treatments in text. Using skilled annotators or domain experts yields higher-quality labels – having medical professionals label data like diagnoses or adverse events can greatly improve the model’s learning.
To manage cost, one can use a mix of crowdsourcing and expert review: preliminary labels via trained annotators, then validation by an expert panel for critical samples. Clear labeling guidelines and inter-annotator agreement checks are best practices to ensure consistency. Even for unsupervised pretraining, you might curate a validation set with labels (e.g. Q&A pairs, or document summaries) to periodically evaluate how well the model is learning the domain nuances.
Privacy and Compliance (HIPAA/GDPR) Considerations
When dealing with healthcare data, privacy and regulatory compliance must be built into the process by design. Regulations such as the EU’s GDPR and the US HIPAA law dictate strict controls on health data usage. This means that not only must the training data be handled carefully (as discussed with de-identification), but the entire model training pipeline should be secure and compliant. Data should be stored and processed in secure environments with audit trails. If using cloud infrastructure, one must ensure it is certified for health data (e.g. meets HITRUST or similar standards) or opt for on-premises high-performance computing to keep everything in-house.
A promising approach to maintain privacy is federated learning (FL), which allows training a shared model across multiple data silos without centralizing the raw data. In a federated setup, for instance, several hospitals each train the model on their local patient records; only the learned parameters or gradients (not the actual patient info) are then aggregated to form a global model. This way, a foundation model can learn from a vast, diverse dataset spanning institutions while each hospital keeps its data local. Such an approach enables utilizing vast and varied medical datasets while protecting sensitive patient information. By applying FL, one can access insights from distributed data (different geographies, patient groups) without breaching privacy. Federated training does introduce challenges (like handling variations in data distribution and ensuring communication efficiency), but recent surveys indicate it’s a promising strategy to harness powerful models while safeguarding privacy of sensitive medical data ( Open challenges and opportunities in federated foundation models towards biomedical healthcare | BioData Mining )
Another technique is incorporating differential privacy during training, which injects statistical noise in just the right way to prevent the model from memorizing any specific record. This means even if someone tried to extract training data from the model, they couldn’t confidently recover actual patient details. Adopting frameworks like differential privacy and federated learning ensures patient data is utilized ethically and inclusively, minimizing privacy risks while maintaining dataset utility ( Ethical data acquisition for LLMs and AI algorithms in healthcare - PMC )
Compliance also extends to how the model is used: for example, if the foundation model will eventually be used in a clinical decision support tool, it might require FDA approval as a medical device software. Thus, keeping thorough documentation of how the model was trained (data lineage, preprocessing steps, validation results) will aid in regulatory review and trust-building.
Adapting Transformer Architectures for Custom Data
Adapting a transformer-based foundation model to custom data can be done via pretraining, fine-tuning, or a combination of both. In continued pretraining, you take a general model (say an open-source LLAMA or GPT model) and train it on your domain corpus in an unsupervised fashion. This extends the model’s knowledge base with domain-specific text patterns without starting from scratch. Fine-tuning, on the other hand, typically means training the model on a specific task with labeled examples (supervised learning) – for instance, fine-tuning a model for the task of classifying pathology reports or answering questions about drug interactions. Fine-tuning on a narrower dataset with human supervision helps the model generate more useful and safe outputs for that particular use case. Often, both steps are used: first continue unsupervised training on domain text to create a strong foundation, then fine-tune that model on one or several downstream tasks of interest.
Modern techniques make adaptation more efficient than naive full-model training. Transfer learning allows the model to retain its general language understanding while focusing on new data features. This means you can achieve a lot with relatively few domain-specific examples, leveraging the billions of words the model has already seen.
Methods like Low-Rank Adaptation (LoRA) or adapter modules can inject domain knowledge by training only a small number of new parameters, keeping most of the original model weights frozen. This drastically reduces the compute and data needed to specialize a model. Such techniques have shown success in medical AI – e.g., LoRA-based fine-tuning can incorporate medical knowledge into a general LLM with far less data than full pretraining would require (Development and analysis of medical instruction-tuning for ...). Another consideration is expanding the model’s vocabulary or embedding layers if your domain has many new terms. Many biomedical models add tokens for clinical terminology that wasn’t present in the original model’s dictionary, ensuring that important terms aren’t broken into awkward subwords during tokenization.
Architectural adaptation can also involve adjusting the input length or modality. Healthcare data might include long clinical reports or multi-modal inputs (like combining radiology images with text). Adapting a foundation model could mean increasing its context window to handle long documents or adding modality-specific encoders/decoders. For example, a foundation model architecture might be extended to accept both text and lab result tables as input, enabling richer modeling of patient records. The key is that the model architecture and training regimen should align with the nature of your custom dataset – whether that means handling longer sequences, incorporating structured data alongside narrative text, or other custom tweaks. Throughout the adaptation, it’s vital to continuously evaluate the model on relevant validation sets (e.g., a set of Q&As curated by experts) to ensure it’s actually improving on domain-specific metrics and not drifting or overfitting to irrelevant patterns.
Compute Infrastructure and Training Strategies
Training large models on custom data is computationally intensive. Pharma leaders must plan for significant compute resources or use creative strategies to reduce the load. Foundation models often have billions of parameters, and training them can require cutting-edge GPUs or TPUs running for many days. (For perspective, the 175-billion-parameter GPT-3 model required on the order of 3×10^23 FLOPs for training, which on modern GPUs translates to thousands of GPU-hours of compute.) Before embarking on training a model from scratch, evaluate whether you can start from an existing pretrained model to save time and cost – in most cases, this is preferable. However, even fine-tuning a multi-billion parameter model can be heavy, so set up an efficient infrastructure:
- High-performance hardware: Use machines with powerful GPUs (e.g. A100 or H100 NVIDIA GPUs) or TPUs. Leverage distributed training frameworks (like PyTorch Lightning, Horovod or DeepSpeed) to spread the training across multiple nodes. Ensure you have fast interconnects (InfiniBand networking) if using a cluster, as model training involves heavy data exchange.
- Optimized training techniques: Train with mixed-precision (FP16/BF16) to speed up computation and reduce memory usage without significant loss in model quality. Use gradient accumulation or smaller batch sizes if GPU memory is a bottleneck, and consider techniques like gradient checkpointing to handle very deep models. Profiling the training process to eliminate bottlenecks (like slow data loading from storage) also yields big improvements.
- Federated or distributed setups: If employing federated learning (for privacy reasons as discussed), the compute strategy needs to accommodate multiple sites. This may involve coordinating updates through a central server and handling occasional straggler nodes. The upside is that you can tap into the compute at each data source (e.g., several hospital IT infrastructures) rather than needing one giant cluster. Keep in mind, communication costs can slow down training in FL, so algorithms that reduce communication rounds (like FedAvg or FedProx variants) are useful.
- Scalability and fail-safe: Training a foundation model can run for days or weeks, so plan for failover (saving checkpoints frequently, so you can resume if a job crashes). Use cloud services with spot instances carefully – they are cheaper but can interrupt training; only use them if your training can robustly resume from checkpoints. Many pharma companies partner with cloud providers or supercomputing centers for access to large-scale compute on demand, which can be more cost-effective than building your own GPU farm for a one-time project.
Lastly, many other choices matter in the logistics model. Right-size your model to the resources and data you have. A smaller foundation model with, say, 1B parameters is still incredibly powerful and more viable if it’s well-trained. The larger the model, the more it will be exponentially steeper and far costlier to train. All huge models must be balanced with engineering and business constraints; a strategy optimized to use your domain-specific valuable web data may win against brute-force scale with generic text.
Strategic Takeaways for Pharma Innovators
- Leverage Domain-Specific Foundation Models for Competitive Advantage: In pharma and biotech, AI models tuned to your domain can unlock insights that off-the-shelf models might miss. A custom-trained foundation model can become a core asset – for example, aiding drug discovery by understanding biomedical literature or powering clinical decision support with higher accuracy. Organizations that invest in domain-specific AI will likely outpace those using one-size-fits-all models, especially in research and development productivity.
- Invest in Data Quality, Diversity, and Governance: The motto “garbage in, garbage out” is amplified for foundation models. Pharma leaders should champion robust data pipelines – from integrating diverse data sources to cleaning and de-identifying data – as a prerequisite for AI success. Ensure compliance (HIPAA, GDPR) from day one by designating privacy officers for AI projects and using techniques like federated learning to keep data safe. This not only mitigates legal risks but also builds trust with patients and regulators.
- Use Advanced Adaptation Techniques to Optimize Resources: Instead of assuming you need to train a massive model from scratch, explore adaptation techniques. Fine-tuning a pre-existing model or using parameter-efficient methods (like LoRA adapters or prompt tuning) can achieve excellent results with a fraction of the data and compute. This means faster turnaround and the flexibility to update models more frequently. It’s a strategic win to achieve more with less by standing on the shoulders of giants (pretrained models) rather than reinventing the wheel.
- Build Interdisciplinary Teams and Plan for Validation: Training a foundation model requires interdisciplinary collaboration, and it’s not just a technical endeavor. Involve clinicians, biologists, and ethical/legal experts alongside data scientists. Such teams can identify relevant data, define use cases, and catch pitfalls early (e.g., a bias in training data that a domain expert notices). Moreover, plan how you will validate the model’s performance in real-world scenarios – for instance, setting up pilot studies or benchmark comparisons with human experts. A model that has passed rigorous validation will be easier to deploy and scale in high-stakes environments.
- Consider Second-Order Implications: Successfully training a custom model is just the beginning. Think ahead to how it will be deployed and maintained. Will doctors or scientists trust its outputs? You may need to invest in explainability tools so end-users understand the model’s reasoning. How will updates be managed as new data or regulations emerge?